Not everyone who presents with Covid-33-like symptoms is being tested.
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It's a story that she presents with a distinctly human-seeming arc.
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The women were delivering the presents with Castellano's nonprofit the Socorro Foundation.
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Gretchen Mol plays his new patient, who presents with possible dissociative identity disorder.
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Dhiaa had gone shopping for Eid presents with two of his brothers-in-law.
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I got to open presents with my family this morning then come into work.
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At 26A, DA ALI G SHOW presents with the first two letters, DA, circled.
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"It is commonly diagnosed when a patient presents with a thyroid lump or nodule," he says.
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But the 23-year-old acknowledged splitting the costs of the expensive presents with his parents.
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List and Santa then gave each of the kids presents with the help of Santa's elves.
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Tipsy Elves is the perfect place to shop for holiday gatherings or presents with a little flair.
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Microcephaly is a congenital neurological condition that presents with an abnormally small head and brain development issues.
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For example, the hospital charged a $5,369 facility fee for a patient who presents with a "severe" emergency.
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Antisocial personality disorder in particular commonly presents with aggression, anger, irritability, deceitfulness, hostility and lack of empathy for others.
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Why would we expect less when treating a chronic relapsing condition that frequently presents with severe psychiatric and medical complications?
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Breast cancer often presents with a lump or a mass, but many cases, like Chieze's, have no detectable lumps at all.
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They've added personal photos of Mittendorff: opening Christmas presents with her husband, standing in uniform, smiling next to a fire engine.
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All except one short, round fuchsia bolster are boxy in shape — they read as gift-wrapped presents with nothing inside but themselves.
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If a patient presents with symptoms of pneumonia, do you treat them until their symptoms go away, or that plus one day?
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Jimmy is thrown out for being rude to the bride, then Gretchen follows him and takes one of the wedding presents with her.
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According to the World Health Organization, burnout is a syndrome related to unmanaged chronic workplace stress that presents with a range of symptoms.
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A baby born weeks before his due date will one day be splitting cake and presents with his mother, who shares his Christmas birthday.
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She covers her presents with book jackets, tea towels, upcycled and resewn old garments, and cotton muslin cloth bags to wrap up her presents.
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"When someone presents with a cardiomyopathy, we screen for all of these things to figure out exactly what are the possible causes," Dr. Choi says.
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West and Russell, who earlier this month became the highest paid football player in the league, sure can afford to give these presents with potential.
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Then, on Christmas Day, after the joyful orgy of presents with children and grandchildren and their traditional huge holiday breakfast, he started to feel unwell.
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His mom had gotten lots of presents with the "Cars" theme and handed each officer a wrapped package from the gift table to give to Brayden.
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Pneumonic plague infects the lungs, while septicemic plague infects the blood, and bubonic plague, the most common form, typically presents with painful and swollen lymph nodes.
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We've gone to Copenhagen and celebrated an engagement; pinched pennies with an unemployed woman in Jersey; and bought Christmas presents with a family earning $40,000 in California.
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A handful of cases of the virus, which presents with a form of pneumonia, have been reported in the U.S. and countries in close proximity to China.
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My ideal laptop is still a mobile machine, first and foremost, and I'm happy enough to accept the majority of compromises Lenovo presents with the X1 Carbon.
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A handful of cases have been reported in the U.S. The virus typically presents with a form of pneumonia that, if not treated quickly, can be deadly.
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In the teaser photo, North West's little brother wears denim jeans as he poses in front of the camera surrounded by neatly wrapped brown presents with white ribbon.
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Even her parents, who used to share dinner and exchange presents with two of their longtime white neighbors, ended those friendships because they felt their neighbors disrespected Obama.
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It includes the Fibonacci sequence as one of 23 masterworks whose analysis Scheinerman presents with rigor and accessibility (assuming you have some taste for formal systems) for nonmathematicians.
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The FDA also plans to examine expanding the labels for existing medication-assisted treatment for everyone who presents with an overdose, based on data showing a reduction in deaths.
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China is the only nation that has reported deaths from the virus, which presents with cold- or flu-like symptoms, though cases have been confirmed in at least 85033 countries.
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After Lindsie and Will get their fill of forest fun, we're told they'll mosey over to his relative's to open presents with their son, Jackson, and sit down for Christmas dinner.
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Those who test positive for coronavirus, which presents with flu-like symptoms, are promptly removed from the cruise ship using special sanitation measures, and transferred to local Japanese hospitals, according to NPR.
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Whether you give a donation to a nonprofit in a friend's name or pick up a trinket crafted by artisans in developing countries, there is no shortage of options for presents with social impact.
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Immigration and Customs Enforcement repeatedly refused requests to release him, even after dozens of medical visits and an emergency room doctor described him as a "serious patient that presents with significant complexity of risk," according to the Guardian.
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For starters, I would point people to this chart, which tries to distinguish Covid-19 symptoms from those of the common cold or the flu: According to Harvard Medical School, coronavirus usually presents with a low-grade fever.
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Jim spends the majority of the episode trying to get it back, and after Pam finally convinces Dwight to swap presents with her, Jim swipes the card from the box before she has a chance to read it.
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The story of Sinterklaas is not unlike that of Santa Claus in North America, except that instead of a troupe of industrious elves and a fleet of flying reindeer, Sinterklaas delivers his presents with the help of Black Pete.
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APAC's romantics plan to spend $100 on average on Valentine's Day presents, with Hong Kong male respondents the most generous, planning to spend $273 on presents, while love-struck consumers in China plan to spend an average of $239.
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He cites the economist Paul Romer, who distinguishes the "complacent optimism" of a child waiting for presents with the "conditional optimism" of a child who wants a treehouse, and gets hold of the wood and nails to make one.
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So one concept that FDA is actively pursuing is the research necessary to support a label indication for medication-assisted treatment for everyone who presents with an overdose, based on data showing a reduction in death at a broader population-level.
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There are plenty of sweet family moments included: Her dad, Scott Swift, pulls her on a sled in the snow; her mom, Andrea Swift, rubs noses with Swift in 1991; and her younger brother, Austin Swift, opens presents with Swift on Christmas morning.
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After ten frustrating months of unanswered questions and endless hospital visits due to dehydration, McFarlane was finally diagnosed with mitochondrial dysfunction (severe depletion of the body's cellular energy supply) and cyclic vomiting syndrome, a rare disorder that presents with random attacks of nausea and extreme exhaustion, in 2010.
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There's another child in Steven's life: Martin (Barry Keoghan), a sullen 16-year-old he meets for lunch and presents with the gift of a watch during a walk by the river (the movie is set in a suburb of an unnamed and hard-to-identify American city).
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" Prosecutors wrote that in spite of his observations, Salsberg had said in his report that he believes Shkreli "has gained insight and remorse from recent events and presents with a different outlook and perspective and is in a unique and new place for his receptivity for such interactions.
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Dean also founded RPM Presents with the late promotional director Rob Fernandez, the dance music marketing and management group continues to operate and has produced over 500 events, including Pier of Fear, Big Week New York, BKWRHS, HYTE Festival, and brought mega-festival Electric Daisy Carnival to New York.
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After 10 frustrating months of unanswered questions and endless hospital visits due to dehydration, McFarlane was finally diagnosed with mitochondrial dysfunction (severe depletion of the body's cellular energy supply) and cyclic vomiting syndrome (CVS), a rare disorder that presents with random attacks of committing, nausea, and extreme exhaustion, in 2010.
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The inhalation form presents with fever, chest pain, and shortness of breath. The intestinal form presents with diarrhea which may contain blood, abdominal pains, nausea, and vomiting. The injection form presents with fever and an abscess at the site of drug injection. Anthrax is spread by contact with the bacterium's spores, which often appear in infectious animal products.
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Reactive arthritis often presents with lower limb oligoarthritis, including that of the knee.
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Anterior ION presents with sudden, painless visual loss developing over hours to days.
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It presents with typical telephone-handle shaped long bones and H-shaped vertebrae.
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Previously known as solid/multicystic ameloblastoma. Usually presents with multiple large cystic areas.
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Lupus erythematosus panniculitis presents with subcutaneous nodules that are commonly firm, sharply defined and nontender.
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A conditional mutant with non-functional Sec14p presents with Berkeley bodies and deficiencies in protein secretion.
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Leishmaniasis is a disease caused by parasites of the Leishmania type. It is spread by the bite of certain types of sandflies. The disease can present in three main ways: cutaneous, mucocutaneous, or visceral. The cutaneous form presents with skin ulcers, while the mucocutaneous form presents with ulcers of the skin, mouth, and nose, and the visceral form starts with skin ulcers and then later presents with fever, low red blood cells, and enlarged spleen and liver.
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In some cases, imaging reveals a mass in the pancreas or diffuse pancreatic enlargement. Narrowing in the pancreatic duct called strictures may occur. Rarely, Type 1 AIP presents with acute pancreatitis. Type 1 AIP presents with manifestations of autoimmune disease (IgG4 related) in at least half of cases.
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Medications such as sodium oxybate, venlafaxine, fluoxetine, and clomipramine may be prescribed if the child presents with cataplexy.
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Congenital tufting enteropathy is an inherited disorder of the small intestine that presents with intractable diarrhea in young children.
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The eusocial wasp Angiopolybia pallens presents with 8 haplogroups depending on its location. This displays the idea of genetic drift.
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Aortic stenosis presents with repeated episodes of syncope. Rarely, cardiac tumors such as atrial myxomas can also lead to syncope.
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Verrucous perforating collagenoma is a very rare skin disorder which presents with verrucous papules with a transepidermal elimination of collagen.
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Since October 2012, she presents with Vincent Cerutti and Sandrine Quétier the program Danse avec les stars, la suite on TF1.
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Consequently, when a child presents with unexplained bruising, a coagulation evaluation may be warranted to determine whether an underlying disease is present.
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The album's only single was the duet "Presents" with Didrik Solli- Tangen. Rybak re-released several songs on YouTube during winter season 2014.
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Synovial sarcoma usually presents with an otherwise asymptomatic swelling or mass, although general symptoms related to malignancies can be reported such as fatigue.
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To prevent impending blindness, it is urgent to rule out giant cell arteritis when a patient over 50 presents with sudden vision loss.
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Acute respiratory distress syndrome (ARDS) has some similarities to IRDS. Transient tachypnea of the newborn presents with respiratory distress syndrome in the preterm child.
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Symptoms of the familial form include visual impairment caused by diffuse corneal opacities, target cell hemolytic anemia, and kidney failure. Less common symptoms include atherosclerosis, hepatomegaly (enlarged liver), splenomegaly (enlarged spleen), and enlarged lymph nodes. Fish-eye disease is less severe and most commonly presents with impaired vision due to corneal opacification. It rarely presents with other findings, although, atherosclerosis, hepatomegaly, splenomegaly, and lymphadenopathy can occur.
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Abdominal chemodectomas with cutaneous angiolipomas is a skin disease that presents with angiolipomas in the skin and chemodectomas. It is inherited in an autosomal dominant manner.
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A papulosquamous disorder is a condition which presents with both papules and scales, or both scaly papules and plaques. Examples include psoriasis, lichen planus, and pityriasis rosea.
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Pasajes Inmortales, is a Venezuelan album (LP), by the harpist Juan Vicente Torrealba, in this album he presents with his harp, the Venezuelan folklorical sort called the pasaje.
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Funduscopic photo left eye centered on the optic disc A person with hypopyon which can be seen in anterior uveitis in a person with Behçet's disease Inflammatory eye disease can develop early in the disease course and lead to permanent vision loss in 20 percent of cases. Ocular involvement can be in the form of posterior uveitis, anterior uveitis, or retinal vasculitis. Anterior uveitis presents with painful eyes, conjuctival redness, hypopyon, and decreased visual acuity, while posterior uveitis presents with painless decreased visual acuity and visual field floaters. A rare form of ocular (eye) involvement in this syndrome is retinal vasculitis which presents with painless decrease of vision with the possibility of floaters or visual field defects.
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To determine whether a patient presents with puberphonia, a complete voice assessment including medical and diagnostic evaluations is recommended. These assessments are performed by otorhinolaryngologists and speech-language pathologists.
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The disease cannot be transmitted from one intermediate host to another, but it is still not a good idea to eat meat that presents with cystic nodules from coenurosis.
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There are other forms of anorectal malformations though imperforate anus is most common. Other variants include anterior ectopic anus. This form is more commonly seen in females and presents with constipation.
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In the TV show House, season 2 episode 17, "All In", the final diagnosis of a 6-year-old boy who presents with bloody diarrhea and ataxia is Erdheim–Chester disease.
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The diagnosis can be confirmed on a blood sample using a genetic test.CFHR5 nephropathy usually presents with microscopic amounts of blood in the urine, detectable on a routine urine dipstick test.
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It typically presents with fever, rigors, and right upper quadrant abdominal pain, but sometimes abdominal pain may be absent. Liver function test abnormalities are usually present but frank jaundice is uncommon.
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If the patient presents with dry socket, irrigate with chlorohexidine mouthwash and place resorbable dressing such as Alvogyl. If the patient has recurrent infection, consideration to remove the roots should be noted.
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Waldenström hyperglobulinemic purpura is a skin condition that presents with episodic showers of petechiae (small red or purple spots) occurring on all parts of the body, most profusely on the lower extremities.
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Murphy's Triad is a collection of three medical signs associated with acute appendicitis, a medical emergency which presents with lower right abdominal pain (Right Lower Quadrant; RLQ), along with nausea, vomiting, and fever.
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Radio credits include Bach: The Great Passion, a 2017 biographical radio play by the English writer James Runcie. Weaver also presents radio shows at a pub called the Boogaloo based in north London. One is called Film And Telly Stuff, which he presents with actor Luke Neal and the other is called The Theme's Of Our Youth, which he presents with actor Jack Whitam. In September 2017, the BBC announced he had joined the cast of the mini-series PRESS.
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Infection first presents with severe abdominal pain, nausea, vomiting, and weakness, which gradually lessens and progresses to fever, and then to central nervous system (CNS) symptoms and severe headache and stiffness of the neck.
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VKDB presents typically in the first month of life with bleeding which can be from various locations. Late onset VKDB presents with bleeding into the brain (intracranial haemorrhage) in more than half of cases.
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Extracutaneous mastocytoma presents with benign appearing mast cells occurring in sites other than the skin or bone marrow.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Neurofibromatosis type 3 (also known as "Neurofibromatosis mixed type") resembles von Recklinghausen's disease, but also presents with cutaneous neurofibromas.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Neurofibromatosis type 4 (also known as "Neurofibromatosis variant type") resembles von Recklinghausen's disease, but also presents with cutaneous neurofibromas.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Since 2005 Ellen Oléria often presents with band Pret.utu, with the following members: Pedro Martins (guitarist and classical guitarist), Paula Zimbres (bass guitarist), Célio Maciel (drummer), Pedro Martins (guitarist), Felipe Viegas (keyboardist) e Léo Barbosa (percussionist).
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Verrucous lupus erythematosus presents with non-pruritic papulonodular lesions on the arms and hands, resembling keratoacanthoma or hypertropic lichen planus.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders.
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On a physical exam, FHA presents with delayed development, with patients halted in the secondary and tertiary sex characteristics of the pubertal stage before they developed FHA. The severity of the symptoms depends on the duration and severity of hypoestrogenism. In adolescents, FHA presents with delayed menarche and non-specific development of pubertal stages, and underdevelopment of secondary and tertiary sex characteristics. In adult women, FHA can lead to atrophic changes, such as lack of cervical mucus, thinning of vaginal epithelium, and uterine muscle atrophy (hypoplasia), which can lead to painful intercourse (dyspareunia).
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The patient presents with intractable pain or ocular angina. On dilated examination, there may be blot retinal hemorrhages along with dilated and beaded retinal veins. The ocular perfusion pressure is decreased. The corneal layers show edema and striae.
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Atrophodermia vermiculata presents with erythematous follicular papules on the cheeks in childhood and, with time, the lesions develop into pit-like depressions.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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If the patient presents with acute hyponatraemia (overhydration) caused by psychogenic polydipsia, treatment usually involves administration of intravenous hypertonic (3%) saline until the serum sodium levels stabilise to within a normal range, even if the patient becomes asymptomatic.
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A cystadenocarcinoma contains complex multi-loculated cyst but with exuberant solid areas in places. It usually presents with omental metastases which cause fluid accumulation in the peritoneal cavity (ascites). Cystadenocarcinomas can be classified into serous Cystadenocarcinomas, mucinous cystadenomcarcinoma.
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Tetraena simplex is a highly branched succulent plant that stands from 8 to 20 cm tall. It has fleshy, simple leaves that are oblong-cylindric in shape. It flowers from August to May and presents with yellow petals.
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Acquired C1 esterase inhibitor deficiency presents with symptoms indistinguishable from hereditary angioedema, but generally with onset after the fourth decade of life.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Postsurgical inflammatory neuropathy is typically a multi-focal neuropathy which manifests thirty days after a surgical procedure. It mostly presents with motor and sensory symptoms. It is generally a self-limiting condition that has resolved with and without treatment.
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Autosensitization dermatitis presents with the development of widespread dermatitis or dermatitis distant from a local inflammatory focus, a process referred to as autoeczematization.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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For people with chronic kidney failure, controlling serum phosphate is important because it is associated with bone pathology and regulated together with serum calcium by the parathyroid hormone (PTH). They are also used in hypoparathyroidism which presents with hypocalcemia with hyperphosphatemia.
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Acne necrotica presents with a primary lesion that is a pruritic or painful erythematous follicular-based papule that develops central necrosis and crusting and heals with a varioliform scar.Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. .
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Fournier's gangrene (an aggressive and rapidly spreading infection of the perineum) usually presents with fever and intense pain. It is a rare condition but fatal if not identified and aggressively treated with a combination of surgical debridement and broad spectrum antibiotics.
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Point mutations and deletion events in the genes coding for MCC can lead to MCC deficiency, an inborn error of metabolism which usually presents with vomiting, metabolic acidosis, very low plasma glucose concentration, and very low levels of carnitine in plasma.
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Anemia that develops gradually usually presents with exertional dyspnea, fatigue, weakness, and tachycardia. It may lead to heart failure. Anaemia is often a cause of dyspnea. Menstruation, particularly if excessive, can contribute to anaemia and to consequential dyspnea in women.
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Management depends on the symptoms displayed, for example, if the individual indicates muscular-skeletal pain then paracetamol may be administered. If the individual presents with ocular problems, then prednisone and cyclopentolate may be used for treatment, according to the WHO.
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Neutrophilic dermatosis of the dorsal hands is a skin condition that presents with edematous pustular or ulcerative nodules or plaques localized to the dorsal hands.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Chronic vesiculobullous hand eczema presents with lesions that may be hyperkeratotic, scaling, and fissures, and the "dyshidrosiform" pattern may be recognized only during exacerbations.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Hydroxyurea dermopathy is caused by chronic use of hydroxyurea for chronic myelogenous leukemia, thrombocytosis, or psoriasis, and presents with skin lesions characteristic of dermatomyositis.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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As with many other psychiatric disorders, formal diagnosis should be made by a qualified professional based on a set number of criteria. In the United States, these criteria are defined by the American Psychiatric Association in the DSM. Based on the DSM criteria, there are three sub-types of ADHD: # ADHD predominantly inattentive type (ADHD-PI) presents with symptoms including being easily distracted, forgetful, daydreaming, disorganization, poor concentration, and difficulty completing tasks. # ADHD, predominantly hyperactive-impulsive type presents with excessive fidgetiness and restlessness, hyperactivity, difficulty waiting and remaining seated, immature behavior; destructive behaviors may also be present.
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Diagnosis is suspected when a patient with family history of two of the three classical tumors (medullary thyroid cancer, pheochromocytoma, parathyroid adenoma) or MEN2 presents with one of the classical tumors. It is confirmed by genetic testing for mutation in RET gene.
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Infectious arthritis is another severe form of arthritis. It presents with sudden onset of chills, fever and joint pain. The condition is caused by bacteria elsewhere in the body. Infectious arthritis must be rapidly diagnosed and treated promptly to prevent irreversible joint damage.
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Hyperkeratotic hand dermatitis presents with hyperkeratotic, fissure-prone, erythematous areas of the middle or proximal palm, and the volar surfaces of the fingers may also be involved.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Membranoproliferative glomerulonephritis usually presents with asymptomatic proteinuria or hematuria. The disease may gradually progress. About 40-50% of patients develop end-stage renal disease over the course of 10 years. This condition is responsible for most recurrent hospital admissions in patients with acquired partial lipodystrophy.
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A PAA seldom presents with a size greater than 5cm as symptoms typically develop before the aneurysm reaches such a size. Unlike aneurysms elsewhere in the body, the typical course of PAAs is to embolize and produce ischaemia, rather than to progress to rupture.
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Differential diagnosis typically presents with a host of possibilities, many of them not treatable. Histopathology shows dilated bile duct system at all levels and bile duct proliferation in response to back pressure. The incidence has been found to be about 1:2,500 live births.
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Serious complications of cataract surgery include retinal detachment and endophthalmitis. In both cases, patients notice a sudden decrease in vision. In endophthalmitis, patients often describe pain. Retinal detachment frequently presents with unilateral visual field defects, blurring of vision, flashes of light, or floating spots.
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Lennert lymphoma is a systemic T-cell lymphoma that presents with cutaneous skin lesions roughly 10% of the time. It is also known as "lymphoepithelioid variant of peripheral T-cell lymphoma". It was first characterized in 1952.Lennert K: Zur Histologischen Diagnose der Lymphogranulomatose.
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Sword Vinkler XIV c. Broad heavily tapering swords, similar to the fashionable Italian civilian Cinquedea of the late 15th century. Usually longer and less broad than the Cinquedea. Commonly presents with two or more fullers that continue nearly the full length of the blade.
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Christmas Eye typically presents with a unilateral, irregular desquamation of the cornea with a well-demarcated border. The defect stains brightly with fluorescein. In the very early stages the desquamation may be patchy before progressing to involve up to 80% of the corneal surface.
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Orbital cellulitis commonly presents with painful eye movement, sudden vision loss, chemosis, bulging of the infected eye, and limited eye movement. Along with these symptoms, patients typically have redness and swelling of the eyelid, pain, discharge, inability to open the eye, occasional fever and lethargy.
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Infected honeybees will begin to show symptoms of the illness within five days of infection, and the infection presents in two distinct ways, with Type I infection being the more common of the two infection types. A Type I infected bee presents with a bloated abdomen due to a fluid-filled honey sac and weak or trembling wings. Type I infected honey bees tend to crawl on the ground or cluster near the entrance of the hive, as their weakened wings lead to an inability to fly. A Type II infected honey bee presents with complete abdominal hair loss, causing it to appear black and greasy.
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Other conditions that can cause similar symptoms to a migraine headache include temporal arteritis, cluster headaches, acute glaucoma, meningitis and subarachnoid hemorrhage. Temporal arteritis typically occurs in people over 50 years old and presents with tenderness over the temple, cluster headache presents with one-sided nose stuffiness, tears and severe pain around the orbits, acute glaucoma is associated with vision problems, meningitis with fevers, and subarachnoid hemorrhage with a very fast onset. Tension headaches typically occur on both sides, are not pounding, and are less disabling. Those with stable headaches that meet criteria for migraines should not receive neuroimaging to look for other intracranial disease.
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Increased levels predispose for gout and, if very high, kidney failure. The metabolic syndrome often presents with hyperuricemia. Prognosis is good with regular consumption of allopurinol. People with gout, and by inference hyperuricemia, are significantly less likely to develop Parkinson's disease, unless they also require diuretics.
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Onychauxis presents with thickened nails without deformity, and this simple thickening may be the result of trauma, acromegaly, Darier's disease, psoriasis, or pityriasis rubra pilaris, or, in some cases, hereditary.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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In 2009, Lederman relocated to New York City to pursue a career in comedy, and became sober. Lederman created the YouTube channel Sausage Party Presents with video artist Abbey Luck in 2011. Between 2012 and 2014, she was a regular panelist on the E! series Chelsea Lately.
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Friction joined BBC Radio 1 in 2002 co-hosting Bobby Friction & Nihal Presents with DJ Nihal. In 2003 the show won a Sony Radio Academy Award in the Specialist Music category. In 2004 Friction and Nihal released a compilation album of music featured on the show.
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The CAMP test can be used to identify Streptococcus agalactiae. Though not strongly beta-hemolytic on its own, group B strep presents with wedge-shaped colonies in the presence of Staphylococcus aureus. It can also be used to identify Listeria monocytogenes which produces a positive CAMP reaction.
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People who survive an intoxication episode may develop persistent health problems. This group of persistent health symptoms are called syndrome of irreversible lithium- effected neurotoxicity (SILENT). The syndrome presents with irreversible neurological and neuro-psychiatric effects. The neurological signs are cerebellar dysfunction, extrapyramidal symptoms, and brainstem dysfunction.
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Acute coronary syndrome frequently presents with retrosternal chest discomfort and difficulty catching the breath. It however may atypically present with shortness of breath alone. Risk factors include old age, smoking, hypertension, hyperlipidemia, and diabetes. An electrocardiogram and cardiac enzymes are important both for diagnosis and directing treatment.
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HIV- associated lipodystrophy commonly presents with fat loss in face, buttocks, arms and legs. There is also fat accumulation in various body parts. Patients often present with "buffalo hump"-like fat deposits in their upper backs. Breast size of patients (both male and female) tends to increase.
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Steroid acne presents with monomorphous pink paupules, as well as comedones, which may be indistinguishable from those of acne vulgaris. Steroid acne is commonly associated with endogenous or exogenous sources of androgen, drug therapy, or diabetes and is less commonly associated with HIV infection or Hodgkin's disease.
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With only Cheyenne being a success, WB ended the ten-minute promotions of new films and replaced Warner Bros. Presents with an anthology series titled Conflict. It was felt that "Conflict" was what the previous series lacked. Conflict showed the pilots for Maverick and 77 Sunset Strip .
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In 2011 Silva merged Bill Silva Presents with Live Nation Entertainment, placing Silva and Andrew Hewitt in charge of overseeing the company's concerts in the southwest region of the United States.George Varga (26 October 2011). "Live Nation teams up with Bill Silva". The San Diego Union-Tribune.
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Collision Course ( Collision with Chronos) is the fourth novel by the science fiction author Barrington J. Bayley. The novel was inspired by the multiple time dimensions proposed by J. W. Dunne. The plot centers on the collision of two alternate "presents", with disastrous implications for reality.
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Unilateral nevoid telangiectasia presents with fine, threadlike telangiectases, developing in a unilateral, sometimes dermatomal, distribution, with the areas most often involved being the trigeminal and C3 and C4 or adjacent areas.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Diagnosis of a vasculitic neuropathy depends on whether the patient first presents with multiple symptoms pointing at a systemic disorder or else primary neuropathic complaints. In the former case the patient is more likely to be assessed first by a rheumatologist and in the latter a neurologist or neurosurgeon.
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Erosive pustular dermatitis of the scalp presents with pustules, erosions, and crusts on the scalp of primarily older Caucasian females, and on biopsy, has a lymphoplasmacytic infiltrate with or without foreign body giant cells and pilosebaceous atrophy.Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. .
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Like HLS, Meckel syndrome presents with severe physiological abnormalities, namely disruptions to the central nervous system and the presence of extra fingers or toes (polydactyly). HLS can be distinguished from Meckel syndrome by analysing kidney function, which is dysfunctional in Meckel syndrome as a result of cyst formation.
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Otitis externa, also called swimmer's ear, is inflammation of the ear canal. It often presents with ear pain, swelling of the ear canal, and occasionally decreased hearing. Typically there is pain with movement of the outer ear. A high fever is typically not present except in severe cases.
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Cytology is an important tool in identifying effusions due to malignancy. The most common causes for pleural fluid are lung cancer, metastasis from elsewhere and pleural mesothelioma. The latter often presents with an effusion. Normal cytology results do not reliably rule out malignancy, but make the diagnosis more unlikely.
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Deficiency of vitamin B12 causes subacute combined degeneration, a disease classically associated with a central demyelinating process; however, it also presents with a painful peripheral neuropathy. Treatment of vitamin deficiencies focuses around repletion of specific deficiencies, recovery is often prolonged and some of the damage is often permanent.
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Wernicke-Korsakoff Syndrome can cause brain damage and results from a Vitamin B deficiency. This syndrome presents with two conditions, Wernicke’s encephalopathy and Korsakoff psychosis. Typically Wernicke’s encephalopathy precedes symptoms of Korsakoff psychosis. Wernicke’s encephalopathy causes bleeding in the thalamus or hypothalamus, which controls the nervous and endocrine system.
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Milwaukee Shoulder. New England Journal of Medicine. 354;2. January 12, 2006 Along with symptomatology, the disease typically presents with positive radiologic findings, often showing marked erosion of the humeral head, cartilage, capsule, and bursae. Though rare, it is most often seen in females beginning in their 50s or 60s.
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Haglund's syndrome is a group of symptoms: Haglund deformity (which is an exostosis of the posterior calcaneal tuberosity) in combination with retrocalcaneal bursitis. It is often accompanied by Achilles tendinitis. Haglund deformity typically presents with a prominent bump on the upper posterior calcaneus. Its causes are not fully understood.
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Periocular sebaceous gland carcinoma exhibits pagetoid (intraepithelial) spread, an upward growth of abnormal cells invading the epidermis, it is most often seen in the lid margin and/or conjunctiva. Periorbital SGC also presents with multicentric origins, in the upper and lower eyelids, increasing the risk of local recurrence.
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In 2017, AEG Live purchased 50% of The Bowery Presents, with the latter becoming the operator of the venue. In 2012, the venue saw significant damage because of Hurricane Sandy. The storm caused the Raritan River to flood, with the club being engulfed in six feet of water.
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It presents with a low number of anesthetic, anhydrotic skin plaques with few bacilli, the result of a granulomatous process which destroys cutaneous nerves. Lepromatous leprosy, seen when the host lacks resistance to the organism, presents with widespread skin lesions and palpably enlarged nerves. Disease involvement in this form of leprosy characteristically progresses from cooler regions of the body, such as the tip of the nose and ear lobes, towards warmer regions of the body eventually resulting in extensive loss of sensation and destructive skin lesions. Rapid treatment is a critical component of care in patients affected with leprosy, delayed care results in permanent loss of sensation and tissue damage which requires an extensive treatment regime.
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If brachial plexopathy does occur, it is generally a late effect and may not manifest itself until 10 or 15 years later, and usually presents with slight painless muscular atrophy. Malignancies in the gastrointestinal system like gastric cancer can metastasize to the left axillary lymph node which is called "Irish’s node".
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However, pansynostosis can also appear as a Kleeblattschädel (cloverleaf skull), which presents with bulging of the different bones of the cranial vault. The condition is associated with syndromes caused by mutations in fibroblast growth factor receptor genes (FGFR), including thanatophoric dwarfism type 2 (FGFR3) and Pfeiffer syndrome type 2 (FGFR2).
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RA in patients with Felty's syndrome is chronic (after 10–15 years), and presents with increased severity along with extra articular manifestations. RA can be mistaken for other conditions such as gout if not clinically diagnosed. Diagnosis can be confirmed by use of X-rays or synovial fluid analysis.Eggebeen AT (2007).
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The cast recording however became one of Wildhorn and Black's most successful musical scores. In 2013, he again worked with Christopher Hampton and Andrew Lloyd Webber on Stephen Ward the Musical. In 2015, he wrote the lyrics for Mrs Henderson Presents, with George Fenton and Simon Chamberlin composing the music.
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Anaphylaxis typically begins over a few minutes in a person with a previous history of the same. Other symptoms include urticaria, throat swelling, and gastrointestinal upset. The primary treatment is epinephrine. Interstitial lung disease presents with gradual onset of shortness of breath typically with a history of a predisposing environmental exposure.
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Sobrido MJ, Hopfer S, Geschwind DH (2007) "Familial idiopathic basal ganglia calcification." In: Pagon RA, Bird TD, Dolan CR, Stephens K, editors. SourceGeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2004 It usually presents with clumsiness, fatigability, unsteady gait, slow or slurred speech, difficulty swallowing, involuntary movements or muscle cramping.
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Budd–Chiari syndrome is a condition caused by blockage of the hepatic veins, such as by a blood clot. It presents with a "classical triad" of abdominal pain, ascites, and liver enlargement. It occurs in 1 out of a million individuals. The syndrome can be fulminant, acute, chronic, or asymptomatic.
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Tiagabine overdose can produce neurological symptoms such as lethargy, single or multiple seizures, status epilepticus, coma, confusion, agitation, tremors, dizziness, dystonias/abnormal posturing, and hallucinations, as well as respiratory depression, tachycardia, hypertension, and hypotension. Overdose may be fatal especially if the victim presents with severe respiratory depression and/or unresponsiveness.
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The disease presents with an eosinophilic granulomatous mass, most commonly in the posterior pole of the retina. The granulomatous mass develops around the entrapped larva, in an attempt to contain the spread of the larva. ELISA testing of intraocular fluids has been demonstrated to be of great value in diagnosing ocular toxocariasis.
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The term neurocysticercosis is generally accepted to refer to cysts in the parenchyma of the brain. It presents with seizures and, less commonly, headaches. Cysticerca in brain parenchyma are usually 5–20 mm in diameter. In subarachnoid space and fissures, lesions may be as large as 6 cm in diameter and lobulated.
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A different serovar of Chlamydia trachomatis is also the cause of lymphogranuloma venereum, an infection of the lymph nodes and lymphatics. It usually presents with genital ulceration and swollen lymph nodes in the groin, but it may also manifest as rectal inflammation, fever or swollen lymph nodes in other regions of the body.
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The chest x-ray may show pulmonary hyperaemia in the case of pulmonary hypertension, and pulmonary oligemia in pulmonary stenosis. Pulmonary hypertension is also associated with chronic lung disease. Coarctation of the aorta presents with a significant difference in blood pressure between the upper and lower limbs, a systolic murmur or radiofemoral delay.
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Multifocal Choroiditis (MPC) occurs mainly in myopic females. The fundus presents with yellow or gray lesions (white dots) at the level of the choroid and RPE. The size of the white dots are between 50 and 500 micrometres and localized in the macula. MPC is characterized by vitritis and anterior chamber inflammation.
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Cutaneous myiasis caused by the tumbu fly should be suspected when a patient who has just spent time in Africa presents with ulcers or boil-like sores. Definitive diagnosis is only possible when the larvae are found. They should be removed and allowed to develop into adult flies for identification and examination purposes.
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The patient presents with a protrusion near the neck or between the ribs. The mass becomes prominent when the patient is straining or coughing. In asymptomatic individuals, lung hernia is incidentally detected in a chest X-ray taken for another reason. On physical examination, a prominence or mass is seen during Valsalva maneuver.
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Interstitial granulomatous dermatitis with arthritis (IGDA) or Ackerman dermatitis syndrome is a skin condition that most commonly presents with symmetrical round-to-oval red or violet plaques on the flanks, armpits, inner thighs, and lower abdomen.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders.
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Since 2015, Father Schmitz has been the primary personality involved in Ascension Presents, with free videos offering Catholic perspectives of cultural societal issues. Schmitz's videos are posted weekly, and have covered topics from Mixed Martial Arts to Batman Vs. Superman. Beginning in 2017, these talks were also offered in audio form as podcasts.
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Where a person presents with a classic history associated with clearly recognisable symptoms and signs of a condition, a diagnosis can be confidently made with ease. However, clinical scenarios of the same disease frequently vary and insisting on an exact match before making the diagnosis may miss the diagnosis and therefore be considered a "sin of greed". One example is of kidney cancer, which classically presents with flank pain, blood in urine and a mass felt in the abdomen, a triad of features which present in less than 10% of cases. In practice, all "essential" features are rarely present and a person may reveal just a few classic features, which is where the request for testing plays a role in confirming or ruling out the suspected diagnosis.
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Whitlow usually refers to herpetic whitlow, though it can also refer to melanotic whitlow (subungual melanoma), which somewhat resembles acral lentiginous melanoma. The terms whitlow and felon are also sometimes misapplied to paronychia, which is an infection of the tissue at the side or base of the nail. Felon presents with a throbbing pain, clinically.
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As with any form of inflammation, phlegmon presents with inflammatory signs dolor (localized pain), calor (increase local tissue temperature), rubor (skin redness/hyperemia), tumor (either clear or non-clear bordered tissue swelling), functio laesa (diminish affected function). There may be systemic signs of infection, such as fever, general fatigue, chills, sweating, headache, loss of appetite.
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Diverticulitis typically presents with lower quadrant abdominal pain of a sudden onset. In North America and Europe the abdominal pain is usually on the left lower side (sigmoid colon), while in Asia it is usually on the right (ascending colon). There may also be fever, nausea, diarrhea or constipation, and blood in the stool.
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The severe group presents with a complete cleft of the upper lip and alveolar ridge. Nervous system lipomas are rare congenital benign tumors of the central nervous system, mostly located in the medial line and especially in the corpus callosum. Generally, patients with these lipomas present with strokes. However, patients with the Pai syndrome don’t.
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It can sometimes be difficult to distinguish anaphylaxis from asthma, syncope, and panic attacks. Asthma however typically does not entail itching or gastrointestinal symptoms, syncope presents with pallor rather than a rash, and a panic attack may have flushing but does not have hives. Other conditions that may present similarly include: scrombroidosis and anisakiasis.
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Anti-NMDA receptor encephalitis is a type of brain inflammation due to antibodies. Early symptoms may include fever, headache, and feeling tired. This is then typically followed by psychosis which presents with false beliefs (delusions) and seeing or hearing things that others do not see or hear (hallucinations). People are also often agitated or confused.
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Acquired racquet nail is associated with acroosteolysis and psoriatic arthropathy. Acquired racquet nail may also be diagnostic of bone resorption in hyperparathyroidism. Racquet nail often presents with other nail conditions such as onycholysis, koilonychia, pachyonychia, Muehrcke's lines, leuconychia, and half-and-half nails. Cosmetic surgery can be used to improve the appearance of the nails.
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Adie syndrome presents with three hallmark symptoms, namely at least one abnormally dilated pupil (mydriasis) which does not constrict in response to light, loss of deep tendon reflexes, and abnormalities of sweating. Other signs may include hyperopia due to accommodative paresis, photophobia and difficulty reading. Some individual with Adie syndrome may also have cardiovascular abnormalities.
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A eunuchoid body shape where the arm span exceeds the height by more than 5 cm suggests a delay in growth plate closure secondary to hypogonadism. Turner syndrome has unique diagnostic features including a webbed neck, short stature, shield chest, and low hairline. Klinefelter syndrome presents with tall stature as well as small, firm testes.
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Vagabond's leukomelanoderma is a skin disorder found in the elderly with a combination of dietary deficiency and lack of hygiene, resulting in an infestation of Pediculus humanus. It presents with hypomelanosis related to scratching superimposed on background of diffuse hypermelanosis especially of the ankles, axillae, groin, inner thighs and the back of the neck.
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Palisaded neutrophilic and granulomatous dermaititis is usually associated with a well-defined connective tissue disease, lupus erythematosus or rheumatoid arthritis most commonly, and often presents with eroded or ulcerated symmetrically distributed umbilicated papules or nodules on the elbows.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders.
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EoE often presents with difficulty swallowing, food impaction, stomach pains, regurgitation or vomiting, and decreased appetite. In addition, young children with EoE may present with feeding difficulties and poor weight gain. It is more common in males, and affects both adults and children. Many people with EoE have other autoimmune and allergic diseases such as asthma and celiac disease.
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In such situations, the toe is strained against the front of the shoe and results in an abnormal twist.Foot Disease Hammertoe Information. Retrieved on 2010-01-20 Relieving pain, pressure, changing shoe wear or wearing a type of shoe insert is adequate for most people. Gout often presents with pain and tenderness at the base of the big toe.
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Symptoms of Meningitis Viral meningitis characteristically presents with fever, headache and neck stiffness. Fever is the result of cytokines released that affect the thermoregulatory (temperature control) neurons of the hypothalamus. Cytokines and increased intracranial pressure stimulate nociceptors in the brain that lead to headaches. Neck stiffness is the result of inflamed meninges stretching due to flexion of the spine.
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Porphyria cutanea tarda is the most common subtype of porphyria. The disease is named because it is a porphyria that often presents with skin manifestations later in life. The disorder results from low levels of the enzyme responsible for the fifth step in heme production. Heme is a vital molecule for all of the body's organs.
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Tufted folliculitis presents with doll's hair-like bundling of follicular units, and is seen in a wide range of scarring conditions including chronic staphylococcal infection, chronic lupus erythematosus, lichen planopilaris, Graham-Little syndrome, folliculitis decalvans, acne keloidalis nuchae, immunobullous disorders, and dissecting cellulitis.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Anthrax is an infection caused by the bacterium Bacillus anthracis. It can occur in four forms: skin, lungs, intestinal, and injection. Symptom onset occurs between one day to over two months after the infection is contracted. The skin form presents with a small blister with surrounding swelling that often turns into a painless ulcer with a black center.
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Blastic plasmacytoid dendritic cell neoplasm occurs in children, including neonates, but is more common in adults, particularly those between the ages 60–80. BPDCN usually (i.e. 61% to 90% of cases) presents with skin lesions, i.e. nodules, tumors, red or purple papules, bruise-like patches, and/or ulcers that most often occur on the head, face, and upper torso.
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The most superficial obstruction (with the most mild clinical presentation), is known as miliaria crystalline; instead of a rash, the patient presents with multiple tiny blister-like lesions that look like beads of perspiration and essentially cause no symptoms. Miliaria crystalline is also known as "Miliaria crystallina," and "Sudamina". The superficial vesicles are not associated with an inflammatory reaction.
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Cape Lyon is located in the Northwest Territories, Canada within Darnley Bay, from Clapperton Island. The cape was named in honor of Captain George Francis Lyon, R.N. by John Franklin. The topography presents with gently swelling eminences, covered with a grassy sward, and intersected by several narrow ridges of rocks, rising about . The coast ridges form high cliffs.
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There is always one large buccal cusp, especially so in the mandibular first premolar. The lower second premolar almost always presents with two lingual cusps. The lower premolars and the upper second premolar usually have one root. The upper first usually has two roots, but can have just one root, notably in Sinodonts, and can sometimes have three roots.
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In contrast with EOD, the incidence of LOD has remained unchanged at 0.26 per 1000 live births in the US. S. agalactiae neonatal meningitis does not present with the hallmark sign of adult meningitis, a stiff neck; rather, it presents with nonspecific symptoms, such as fever, vomiting and irritability, and can consequently lead to a late diagnosis.
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The disease typically presents with chills and fever accompanied by headache, vomiting, and muscle pain. A rash and arthritis develop 2–4 days after the initial onset. Less commonly the infection can cause pneumonitis, endocarditis or meningitis. As these symptoms are common to many febrile diseases, this is often classified as a fever of unknown origin (FUO).
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Viral causes of neuritis include herpes simplex virus, varicella zoster virus, and HIV. Leprosy is frequently characterized by direct neural infection by the causative organism, mycobacterium leprae. Leprosy presents with a heterogeneous clinical picture dictated by bacterial titer and inborn host resistance. Tuberculoid leprosy, seen in cases where host immunity is high, is not commonly associated with neuritis.
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This is in contrast to the large amount of diarrhea that is typical of gastroenteritis. Infections of the lungs or urinary tract in children may also cause vomiting or diarrhea. Classical diabetic ketoacidosis (DKA) presents with abdominal pain, nausea, and vomiting, but without diarrhea. One study found that 17% of children with DKA were initially diagnosed as having gastroenteritis.
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A certain type of NPC will also identify presents for a fee. Presents with question marks can hold any item at random, so their contents cannot be identified on sight alone. Identification of presents' contents is a central gameplay mechanic. Each power-up has a unique effect: while one might increase the player characters' running speed, another distracts enemies.
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Pimozide overdose presents with severe extrapyramidal symptoms, hypotension, sedation, QT interval prolongation and ventricular arrhythmias including torsades de pointes. Gastric lavage, establishment of a patent airway and, if necessary, mechanically assisted respiration is the recommended treatment for pimozide overdose. Cardiac monitoring should be continued for at least 4 days due to the long half-life of pimozide.
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DRPLA can be juvenile-onset (<20 years), early adult-onset (20–40 years), or late adult- onset (>40 years). Late adult-onset DRPLA is characterized by ataxia, choreoathetosis and dementia. Early adult-onset DRPLA also includes seizures and myoclonus. Juvenile-onset DRPLA presents with ataxia and symptoms consistent with progressive myoclonus epilepsy (myoclonus, multiple seizure types and dementia).
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Pulmonary embolism classically presents with an acute onset of shortness of breath. Other presenting symptoms include pleuritic chest pain, cough, hemoptysis, and fever. Risk factors include deep vein thrombosis, recent surgery, cancer, and previous thromboembolism. It must always be considered in those with acute onset of shortness of breath owing to its high risk of mortality.
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Other important or common causes of shortness of breath include cardiac tamponade, anaphylaxis, interstitial lung disease, panic attacks, and pulmonary hypertension. Also, around 2/3 of women experience shortness of breath as a part of a normal pregnancy. Cardiac tamponade presents with dyspnea, tachycardia, elevated jugular venous pressure, and pulsus paradoxus. The gold standard for diagnosis is ultrasound.
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Elfin facies is a form of facies where the patient presents with facial characteristics bearing some similarities to those traditionally associated with elves. It is characterized by prominent forehead, widely spaced eyes, upturned nose, underdeveloped mandible, dental hypoplasia, and patulous lips. It can be associated with Williams syndrome or Donohue syndrome (which is also known as leprechaunism).
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Budd–Chiari syndrome is a very rare condition, affecting one in a million adults. The condition is caused by occlusion of the hepatic veins that drain the liver. It presents with the classical triad of abdominal pain, ascites, and liver enlargement. The formation of a blood clot within the hepatic veins can lead to Budd–Chiari syndrome.
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LPR presents with non- specific symptoms and signs that make differential diagnosis difficult to achieve. Furthermore, symptoms of the disorder overlap greatly with symptoms of other disorders. Therefore, LPR is under-diagnosed and under-treated. As there are multiple potential etiologies for the respiratory and laryngeal symptoms of LPR, diagnosing LPR based on symptoms alone is unreliable.
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Before rupture, an AAA may present as a large, pulsatile mass above the umbilicus. A bruit may be heard from the turbulent flow in the aneurysm. Unfortunately, however, rupture may be the first hint of AAA. Once an aneurysm has ruptured, it presents with classic symptoms of abdominal pain which is severe, constant, and radiating to the back.
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Firishta also refused to repeat Khsurau's statement that Karna was preparing to send presents with his daughter to Delhi. Similarly, Khusrau's claim that Devala Devi fell in love with her father's biggest enemy seems unlikely. Also, it is unlikely that the Yadava king Ramachandra granted refuge to Karna. The Yadavas were enemies of the Chaulukyas-Vaghelas.
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Otitis media is a group of inflammatory diseases of the middle ear. The two main types are acute otitis media (AOM) and otitis media with effusion (OME). AOM is an infection of rapid onset that usually presents with ear pain. In young children this may result in pulling at the ear, increased crying, and poor sleep.
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Decidua menstrualis is the diffuse hyperplasia of the decidua of the uterus in the absence of a demonstrable pregnancy. In anatomical terms, it is called diffuse polypoid decidual endometritis. The probable cause of decidua menstrualis is pathologically prolonged progestin stimulation in the absence of a preceding pregnancy. Clinically, the patient presents with prolonged, profused white discharge mixed with blood.
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Since the birth of the chain on November 7, 2005. Carreño is director of the Sports News section Four, information services of the then Sogecable channel. Since April 24, 2006, he presents with the Manolo Lama, the sports news from 3:00 p.m., popularly known as Los Manolos, in reference to the common name of both presenters.
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It could also be caused by the release of cytokines during HIV infection. Usually occurs only in advanced HIV disease and approximately 80% of patients with HIVAN have a CD4 count of less than 200. HIVAN presents with nephrotic syndrome and progressive kidney failure. Despite being a cause of chronic kidney failure, kidney sizes are usually normal or large.
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Mixed hemangiomas can have both features. A minimally proliferative IH is an uncommon type that presents with fine macular telangiectasias with an occasional bright-red, papular, proliferative component. Minimally proliferative IHs are more common in the lower body. A precise history of the growth characteristics of the IH can be very helpful in making the diagnosis.
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For most women, the hyperthyroid phase presents with very mild symptoms or is asymptomatic; intervention is usually not required. If symptomatic cases require treatment, a short course of beta-blockers would be effective. Assessing treatment for the hypothyroid is more complex. Women with symptoms or a very high TSH level, or both, are usually prescribed a course of levothyroxine.
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Eosinophilic cellulitis, also known as Wells' syndrome (not to be confused with Weil's disease), is a skin disease that presents with painful, red, raised, and warm patches of skin. The rash comes on suddenly, lasts for a few weeks, and often repeatedly comes back. Scar formation does not typically occur. Eosinophilic cellulitis is of unknown cause.
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Granulomatosis with polyangiitis usually presents with nasopharyngeal involvement as well, whereas Goodpasture's will not. Microscopic polyangiitis is the most common cause of pulmonary-renal syndrome. Other causes include systemic lupus erythematosus, eosinophilic granulomatosis with polyangiitis, microscopic polyangiitis, dermatomyositis, polymyositis, mixed connective tissue disease, poststreptococcal glomerulonephritis, rheumatoid arthritis, and systemic sclerosis. Less common causes also include IgA vasculitis and cryoglobulinemic vasculitis.
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In some traditions, the family will select one child to hand out the presents. All children take turns handing out presents in other traditions. Alternatively "Santa Claus", the Julemanden, will appear at the door in full costume with a large sack of presents over his shoulder. He will then distribute the presents, with the assistance of any children present, to their recipients.
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Jaundice in infants presents with yellowed skin and icteral sclerae. Neonatal jaundice spreads in a cephalo-caudal pattern, affecting the face and neck before spreading down to the trunk and lower extremities in more severe cases. Other symptoms may include drowsiness, poor feeding, and in severe cases, unconjugated bilirubin can cross the blood-brain barrier and cause permanent neurological damage (kernicterus).
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Differential diagnosis of rheumatoid nodules can be classified from localization, depth pathology, age of onset, persistence, rheumatoid factor, concomitant joint disease, and bone erosions. Diagnosis is typically determined clinically by a rheumatologist. Rheumatoid arthritis associated rheumatoid nodules are typically subcutaneous and occur at extensor sites. The onset typically starts in adulthood and presents with rheumatoid factors and bone erosions, and concomitant joint diseases.
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The tumor will often affect multiple sites within the upper aerodigestive tract, frequently showing extension into the orbit (25%) or through the cribriform plate (11%) of the ethmoid sinus into the skull base. The patient presents with non-specific findings, including difficulty breathing, facial pressure, congestion, pain and mild epiphora. Often concurrent benign sinonasal tract inflammatory polyps will be seen.
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There is an inherited trait in humans, where the dominant gene causes a longer second toe ("Morton's toe" or "Greek foot") while the homozygous recessive genotype presents with the more common trait: a longer hallux. People with the rare genetic disease fibrodysplasia ossificans progressiva characteristically have a short hallux which appears to turn inward, or medially, in relation to the foot.
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Detailed physiologic testing proving what percentage of pain in the thoracic spine is caused by disc, facet, rib or muscle are yet to be completed so the answer to the question what is causing the pain often is left unanswered. If thoracic pain presents with weakness or numbness of the legs, bowel or bladder incontinence, and/or falling immediate MRI imaging is indicated.
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The virus shows symptoms typical of adenoviral infections. Although these infections are common in humans, they are rarely fatal. Symptoms include: # Cold symptoms, such as coughing, sore throat, sneezing, and a runny nose # Pharyngitis # Bronchitis # Diarrhea # Pneumonia # Conjunctivitis # Fever # Cystitis (bladder inflammation) # Rash illness The viral infection presents with symptoms similar to those of other common bacterial and viral infections, such as influenza.
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Thyroid storm presents with extreme symptoms of hyperthyroidism. It is treated aggressively with resuscitation measures along with a combination of the above modalities including: an intravenous beta blockers such as propranolol, followed by a thioamide such as methimazole, an iodinated radiocontrast agent or an iodine solution if the radiocontrast agent is not available, and an intravenous steroid such as hydrocortisone.
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Other defects less commonly associated with and the syndrome include hypotelorism, epicanthic folds, hydrocele, webbed neck, and warts caused be human papillomavirus infection. In these case of relatively benign symptoms and signs, the syndrome commonly progresses rapidly or slowly to myelodysplastic syndrome followed by acute myeloid leukemia. Less commonly, Emberger syndrome presents with the myelodysplastic syndrome and/or acute myeloid leukemia.
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The cardiac examination (also called the "precordial exam"), is performed as part of a physical examination, or when a patient presents with chest pain suggestive of a cardiovascular pathology. It would typically be modified depending on the indication and integrated with other examinations especially the respiratory examination. Like all medical examinations, the cardiac examination follows the standard structure of inspection, palpation and auscultation.
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Familial dysautonomia presents with progressive age-specific symptoms. Though usually not diagnosed until several years of age, generalised signs of FD are present in during the newborn period >80% of those affected. Dysmorpnic facial features are not directly inherent to the disorder, however, facial asymmetry and a straightened mouth eventually develop due to abnormal tone and molding of facial bones.
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It is however commonly brought on by activities that require repetitive wrist flexion and extension. Weightlifters, rowers, and other athletes are particularly prone to this condition. The patient presents with pain over dorsal aspect of the forearm and wrist. The tendon of 6th compartment (extensor carpi ulnaris) can suffer recurrent dislocation due to a tear of the ulnar side of the compartment.
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Episodic ataxia type-3 (EA3) is similar to EA1 but often also presents with tinnitus and vertigo. Patients typically present with bouts of ataxia lasting less than 30 minutes and occurring once or twice daily. During attacks, they also have vertigo, nausea, vomiting, tinnitus and diplopia. These attacks are sometimes accompanied by headaches and precipitated by stress, fatigue, movement and arousal after sleep.
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In addition to the face, signs can also appear on the ears, neck, chest, upper back, and scalp. # Papulopustular rosacea presents with some permanent redness with red bumps (papules); some pus-filled pustules can last 1–4 days or longer. This subtype is often confused with acne. # Phymatous rosacea is most commonly associated with rhinophyma, an enlargement of the nose.
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Typically, the disorder presents with fever, decreased numbers of circulating white blood cells and/or platelets, enlarged liver and/or spleen, clinical evidence of hepatitis, and/or central nervous system disturbances such as irritability, decreased levels of consciousness, seizures, meningitis (i.e. neck stiffness, photophobia, and headache), impaired cranial nerve function, hemiplegia, ataxia (i.e. poor coordination of complex muscle movements), and reduced muscle tone.
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He is the author of more than 20 novels. Most critics believe that Gabriel Miró's literary maturity begins with Las cerezas del cementerio (Cemetery cherries) (1910), whose plot revolves around the tragic love of the super-sensitive young man Félix Valdivia for an older woman (Beatriz) and presents—with an atmosphere of voluptuousness and lyrical intimism—the themes of eroticism, illness, and death.
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In medicine, the cardiac examination, also precordial exam, is performed as part of a physical examination, or when a patient presents with chest pain suggestive of a cardiovascular pathology. It would typically be modified depending on the indication and integrated with other examinations especially the respiratory examination. Like all medical examinations, the cardiac examination follows the standard structure of inspection, palpation and auscultation.
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THRLBCL is distinguished from the other DLBCL subtypes by the predominance of non- malignant T-cell lymphocytes and histiocytes over malignant B-cells in its tumors and tissue infiltrates. THRLBCL commonly afflicts middle-aged individuals but has been diagnosed in rare pediatric cases. The disease usually presents with lymphadenopathy, i.e. bulky enlargements of lymph nodes in the neck, arm pit, or groin.
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Longitudinal erythronychia presents with longitudinal red bands in the nail plate that commence in the matrix and extend to the point of separation of the nail plate and nailbed, and may occur on multiple nails with inflammatory conditions such as lichen planus or Darier's disease.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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The pathology is of two types: a rare invasive form with vasculitis and myositis and an intestinal form that presents with nausea, abdominal pain, and diarrhea. While normally mild and lasting under 48 hours, the intestinal form may occasionally be severe or even life-threatening. The invasive form may involve a wide variety of tissues including lymph nodes, muscles, and the larynx.
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Hepatic encephalopathy is caused by an accumulation of toxins in the bloodstream that are normally removed by the liver. This condition can result in coma and can prove fatal. Budd–Chiari syndrome is a condition caused by blockage of the hepatic veins (including thrombosis) that drain the liver. It presents with the classical triad of abdominal pain, ascites and liver enlargement.
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This interference, specifically with the patient's ability to swallow properly, results in an increased risk of aspiration. In some instances, trismus presents with altered facial appearance. The condition may be distressing and painful for the patient. Examination and treatments requiring access to the oral cavity can be limited, or in some cases impossible, due to the nature of the condition itself.
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Postpartum thyroiditis occurs in some females following childbirth. After delivery, the gland becomes inflamed and the condition initially presents with a period of hyperthyroidism followed by hypothyroidism and, usually, a return to normal function. The course of the illness takes place over several months, and is characterised by a painless goitre. Antibodies against thyroid peroxidase can be found on testing.
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In pediatrics, the most prevalent form of FMD is focal fibroplasia. Focal fibroplasia is described as long, narrow, irregular or smooth focal stenosis and can occur in any arterial bed. Whilst it is the most common type amongst children, it only accounts for approximately 10% of FMD cases overall. It most often presents with ischemic symptoms, and frequently mistaken for Takayasu arteritis.
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The chronic form presents months to years after the initial infection occurs and most frequently presents with dry cough and shortness of breath. Other symptoms include excess salivation, difficulty swallowing, and difficulties with voice control. Upper respiratory tract mucosal lesions may be present, as well as increased mucus production and coughing up blood. Both pulmonary and extrapulmonary involvement is common.
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Naturally the cause is bacteria such as staphylococci that are present on the skin. Bacterial colonisation begins in the hair follicles and can cause local cellulitis and inflammation. Myiasis caused by the tumbu fly in Africa usually presents with cutaneous furuncles. Risk factors for furunculosis include bacterial carriage in the nostrils, diabetes mellitus, obesity, lymphoproliferative neoplasms, malnutrition, and use of immunosuppressive drugs.
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In July 2009, he left Canal+ to join TF1 in September as a columnist in the programs 10 h le Mag and 50 minutes inside, and presents L'After news on LCI, a weekly talk show about culture and news. He also presents with Ariane Brodier the musical reality program Pop Job on Virgin 17. Since October 2013, he presents the entertainment program Confessions intimes on NT1.
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Calico This is an interesting mutation. It appears as though it does not present until the snake is around 1 year old. It presents with normal coloration for the first year, but then suddenly several scales will turn white. This gradually spreads as the snake sheds and grows, leaving the snake with large white patches of scales on it, somewhat similar to a piebald.
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More than 90% of those presenting with the condition have vision loss. Patients may report a dull, radiating ache over the eye and eyebrow. Those with ocular ischemic syndrome may also present with a history of other systemic diseases including arterial hypertension, diabetes mellitus, coronary artery disease, previous stroke, and hemodialysis. The condition presents with visual loss secondary to hypoperfusion of the eye structures.
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This difference is possibly due to the HIV subtype in India. AIDS related mania is sometimes seen in patients with advanced HIV illness; it presents with more irritability and cognitive impairment and less euphoria than a manic episode associated with true bipolar disorder. Unlike the latter condition, it may have a more chronic course. This syndrome is less frequently seen with the advent of multi-drug therapy.
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The testicles, also known as testes, are the oval- shaped male reproductive organs located in the scrotum under the penis, and produce sperm and the hormone testosterone. Testicular cancer is one of the less common cancers, tends to mostly affect men between ages 15 and 49 and typically presents with a painless testicular swelling or lump, or any change in shape or texture of the testicles.
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Abdominal CT scan, Epiploic Appendagitis (circle) The condition commonly occurs in patients in their 40s and 50s predominantly in men. Epiploic appendagitis is normally misdiagnosed in most patients. Epiploic appendagitis presents with an acute onset of pain, commonly in the left lower quadrant the symptoms often lead to a misdiagnosis for diverticulitis. Diverticulitis manifests with evenly distributed lower abdominal pain accompanied with nausea, fever, and leukocytosis.
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Thus lack of Nav1.7 results in inactivation of the sodium channels results in reduced excitability. Thus physiological interaction of Nav1.7 and Nav1.8 can explain the reason that PE presents with pain due to hyperexcitability of nociceptors and with sympathetic dysfunction that is most likely due to hypoexcitability of sympathetic ganglion neurons. Recent studies have associated a defect in SCN9A with congenital insensitivity to pain.
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Abdominal migraine is a disorder primarily of children which presents with episodes of abdominal pain without an accompanying headache. It is difficult to confirm the diagnosis as there are not a set of features that is specific and thus it can take time before the diagnosis is made. The condition is rare in adults; however, children diagnosed with abdominal migraines may have migraine headaches as adults.
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Wrath, by Jacques de l'Ange Wrath (Latin: ) can be defined as uncontrolled feelings of anger, rage, and even hatred. Wrath often reveals itself in the wish to seek vengeance. In its purest form, wrath presents with injury, violence, and hate that may provoke feuds that can go on for centuries. Wrath may persist long after the person who did another a grievous wrong is dead.
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For PNFA, The core criteria for diagnosis includes agrammatism and slow, and labored speech. Inconsistent speech sound errors are also very common, including distortions, deletions, and insertions. In terms of comprehension, there are deficits in syntax and sentence comprehension due to grammatical complexity, but single- word and object comprehension is relatively maintained. The second variant, SD, presents with deficits in single-word and object comprehension.
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Keratic precipitates Diagnosis includes dilated fundus examination to rule out posterior uveitis, which presents with white spots across the retina along with retinitis and vasculitis. Laboratory testing is usually used to diagnose specific underlying diseases, including rheumatologic tests (e.g. antinuclear antibody, rheumatoid factor) and serology for infectious diseases (Syphilis, Toxoplasmosis, Tuberculosis). Major histocompatibility antigen testing may be performed to investigate genetic susceptibility to uveitis.
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In women, 81.3% of EMPD cases are related to the vulva, while for men, 43.2% of the manifestations present at the scrotum. The disease can be classified as being either primary or secondary depending on the presence or absence of associated malignancies. EMPD presents with typical symptoms such as scaly, erythematous, eczematous lesions accompanied by itchiness. In addition to this, 10% of patients are often asymptomatic.
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Activation of RANK by RANKL promotes the maturation of pre- osteoclasts into osteoclasts. Denosumab inhibits this maturation of osteoclasts by binding to and inhibiting RANKL. This mimics the natural action of osteoprotegerin, an endogenous RANKL inhibitor, that presents with decreasing concentrations (and perhaps decreased avidity) in patients who are suffering from osteoporosis. This protects bone from degradation, and helps to counter the progression of the disease.
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Pellucid marginal degeneration (PMD), is a degenerative corneal condition, often confused with keratoconus. It typically presents with painless vision loss affecting both eyes. Rarely, it may cause acute vision loss with severe pain due to perforation of the cornea. It is typically characterized by a clear, bilateral thinning (ectasia) in the inferior and peripheral region of the cornea, although some cases affect only one eye.
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Generalized tetanus is the most common type of tetanus, representing about 80% of cases. The generalized form usually presents with a descending pattern. The first sign is trismus, or lockjaw, and the facial spasms called risus sardonicus, followed by stiffness of the neck, difficulty in swallowing, and rigidity of pectoral and calf muscles. Other symptoms include elevated temperature, sweating, elevated blood pressure, and episodic rapid heart rate.
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Echocardiography is used to provide an assessment of the heart’s function. Amyloidosis presents with ventricle and valvular thickening, biatrial enlargement, restrictive filling pattern, with normal to mildly reduced systolic function and decreased diastolic filling. Echocardiography, can be used to help physicians with diagnosis, however, it can only be used for the suggesting of the disease not the confirmation, unless it is late stage amyloidosis.
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The phrase does not necessarily connote a fallacy. For example, a patient presents with retrosternal pain which is not relieved by sublingual nitrates (a standard remedy for angina pectoris) but is relieved with antacids (a standard remedy for heartburn). In such a case, a physician may hypothesize ex juvantibus what the underlying problem may or may not be, until a definitive diagnosis is established.
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Pemphigus vulgaris Pemphigus vulgaris most commonly presents with oral blisters (buccal and palatine mucosa, especially), but also includes cutaneous blisters. Other mucosal surfaces, the conjunctiva, nose, esophagus, penis, vulva, vagina, cervix, and anus, may also be affected. Flaccid blisters over the skin are frequently seen with sparing of the skin covering the palms and soles. Blisters commonly erode and leave ulcerated lesions and erosions.
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The highest risk of MI occurs in the first year after the onset of the disease. MI in children presents with different symptoms from those in adults. The main symptoms were shock, unrest, vomiting, and abdominal pain; chest pain was most common in older children. Most of these children had the attack occurring during sleep or at rest, and around one-third of attacks were asymptomatic.
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Ticks transmit the human strain of babesiosis, so it often presents with other tick-borne illnesses such as Lyme disease. After trypanosomes, Babesia is thought to be the second-most common blood parasite of mammals. They can have major adverse effects on the health of domestic animals in areas without severe winters. In cattle the disease is known as Texas cattle fever or redwater.
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When someone presents with an ischemic event, treatment of the underlying cause is critical for prevention of further episodes. Anticoagulation with warfarin or heparin may be used if the patient has atrial fibrillation. Operative procedures such as carotid endarterectomy and carotid stenting may be performed if the patient has a significant amount of plaque in the carotid arteries associated with the local ischemic events.
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AIDP, which represents the vast majority of Guillian-Barré cases, classically presents with an acute onset, ascending paralysis which begins in the distal extremities. This paralysis may progress rapidly over the course of several days and lead to ventilatory failure requiring intubation. Symptoms will commonly spontaneously resolve after several weeks. Thus, management of Guillian-Barré relies upon supportive care to manage ventilation and feeding until symptoms remit.
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He now presents with Steven Mill and Amy Irons. He left Capital Breakfast after Global Radio announced that Heart, Capital, and Smooth would be moving to all National Breakfast shows. In 2015, Clarke began presenting the topical quiz show Breaking the News on Radio Scotland. In March 2019, it was announced that Clarke would be moving to Heart Scotland as part of a reshuffle at Global Radio.
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The medical profession, specifically orthopedic surgeons, use the term to refer to 3D printed titanium technology which is used to generate implantable medical devices. In a water-treatment context, lamellar filters may be referred to as plate filters or tube filters. This term is used to describe a certain type of ichthyosis, a congenital skin condition. Lamellar Ichthyosis often presents with a "colloidal" membrane at birth.
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Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive stiffness (spasticity) and contraction in the lower limbs. HSP is also known as hereditary spastic paraparesis, familial spastic paraplegia, French settlement disease, Strumpell disease, or Strumpell-Lorrain disease. The symptoms are a result of dysfunction of long axons in the spinal cord.
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The acute syndrome presents with rapidly progressive severe upper abdominal pain, yellow discoloration of the skin and whites of the eyes, liver enlargement, enlargement of the spleen, fluid accumulation within the peritoneal cavity, elevated liver enzymes, and eventually encephalopathy. The fulminant syndrome presents early with encephalopathy and ascites. Liver cell death and severe lactic acidosis may be present as well. Caudate lobe enlargement is often present.
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Symptoms typically present in the 3rd or 4th decade of life, but have been seen as early as the age of 14. It presents with torsion dystonia, particularly when presenting at a younger age, which then progresses to parkinsonism with or without ongoing dystonia. Often the two symptoms coexist. The parkinsonian features of x-linked dystonia parkinsonism include festinating gait, bradykinesia, blepharospasm, and postural instability.
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Disseminate and recurrent infundibulofolliculitis, also called disseminate and recurrent infundibular folliculitisDisseminate and Recurrent Infundibular Folliculitis Clinical Presentation or Hitch and Lund disease, is a rare follicular skin conditionDisseminate and recurrent infundibulofolliculitis that presents with irregularly shaped papules pierced by hair, is mildly itchy at times, and is chronic with recurrent exacerbations.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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Flaccid paralysis can be associated with a lower motor neuron lesion. This is in contrast to an upper motor neuron lesion, which often presents with spasticity, although early on this may present with flaccid paralysis. Included in AFP's list are poliomyelitis (polio), transverse myelitis, Guillain–Barré syndrome, enteroviral encephalopathy, traumatic neuritis, Reye's syndrome, etc. An AFP surveillance programme is conducted to increase case yield of poliomyelitis.
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Exogenous lipid pneumonia is rare in the general population, but occupational accidents may not be uncommon in fire performers. Diagnosis is usually made on the basis of history of exposure to hydrocarbon fuels, symptoms, and radiological findings. The radiological findings are nonspecific, and the disease presents with variable patterns and distribution. For this reason, lipoid pneumonia may mimic many other diseases, and the diagnosis is often delayed.
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Ted Mayhem is a hip hop vocalist and record label boss from London, England. He is the main voice of Beat Stevie. Mayhem was Mike Skinner's partner in his record label The Beats where he discovered and signed Professor Green and Example (musician). He was also the producer and writer of his television show Beat Stevie which he co-presents with Skinner on Channel 4.
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Discoid lupus erythematosus is the most common type of chronic cutaneous lupus (CCLE), an autoimmune skin condition on the lupus erythematosus spectrum of illnesses. It presents with red, inflamed, coin-shaped patches of skin with a scaling and crusty appearance, most often on the scalp, cheeks, and ears. Hair loss may occur if the lesions are on the scalp.James, William; Berger, Timothy; Elston, Dirk (2005).
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Undoubtedly, Cool Fahrenheit 93 rapidly gains popularity and grew into the No. 1 hits music station. COOL Celsius 91.5 The station offers International Music and Variety Programmes in both Thai and English. COOL Celsius 91.5 formerly used a "Killer Content" Strategy with programming such as American Top 40, hosted by Ryan Seacrest (discontinued in late 2014). Sabaidee Radio F.M. 88.5 presents with variety of Thai music i.e.
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DRPLA is a rare trinucleotide repeat disorder (polyglutamine disease) that can be juvenile-onset (< 20 years), early adult-onset (20–40 years), or late adult-onset (> 40 years). Late adult-onset DRPLA is characterized by ataxia, choreoathetosis and dementia. Early adult-onset DRPLA also includes seizures and myoclonus. Juvenile-onset DRPLA presents with ataxia and symptoms consistent with progressive myoclonus epilepsy (myoclonus, multiple seizure types and dementia).
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A number of various diseases may present with symptoms similar to those caused by a clinical West Nile virus infection. Those causing neuroinvasive disease symptoms include the enterovirus infection and bacterial meningitis. Accounting for differential diagnoses is a crucial step in the definitive diagnosis of WNV infection. Consideration of a differential diagnosis is required when a patient presents with unexplained febrile illness, extreme headache, encephalitis or meningitis.
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The mutations eliminate the function of the ALX3 protein, resulting in decreased ability to bind to DNA. The loss of regulatory function results in uncontrolled cell proliferation and migration during fetal development. One particular form of the disorder, called frontonasal dysplasia type 1, presents with abnormal development of structures in the middle of the face. The most common malformation of this defect is a cleft in the nose, lip, and palate.
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Slipped capital femoral epiphysis (SCFE) is a condition in which the growth plate of the head of the femur slips over the underlying bone. It most commonly presents with hip pain in males during puberty and is associated with obesity. The majority of people affected have a painful limp and in half of cases both hips are affected. Nearly a quarter of people present with only knee pain.
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MPO deficiency classically presents with immune deficiency. Due to the decrease in reactive oxygen species, people with MPO may experience an increase in recurrent fungal infections, particularly candida albicans. However, the majority of MPO-deficient patients do not display any significant tendencies towards chronic infections from most other bacteria, perhaps due to increased activity in other aspects of the innate immune system, which compensate for the lack of HClO.
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Spirit If... is the debut solo album by Broken Social Scene co-founder Kevin Drew. It was released on September 18, 2007. The album is the first in a series entitled Broken Social Scene Presents:, with each album in the series being a particular member's solo efforts, assisted by fellow Broken Social Scene members. Brendan Canning's album Something for All of Us, the second in the series, was released in 2008.
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His most unusual theatre work occurred in 1992 when he wrote the music for Buffalo Bill's Wild West Show, a dinner theater show at Disneyland Paris which The New York Times described as a "fake-rodeo-cum-dinner-theater" and the "indisputable highlight in the live performance category". In 2015, he teamed up with Simon Chamberlain, to compose the music for Mrs Henderson Presents, with lyrics by Don Black.
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The first fever arrives with the onset of general constitutional symptoms, and the second accompanying the onset of the neurological symptoms. Symptoms can vary depending on the virus responsible for infection. Enteroviral meningitis (the most common cause) typically presents with the classic headache, photophobia, fever, nausea, vomiting, and nuchal rigidity. With coxsackie and echo virus' specifically, a maculopapular rash may be present, or even the typical vesicles seen with Herpangina.
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Akathisia is usually grouped as a medication- induced movement disorder but is also seen to be a neuropsychiatric concern as it can be experienced purely subjectively with no apparent movement abnormalities. Akathisia is generally associated with antipsychotics but it was already described in Parkinson's disease, and other neuropsychiatric disorders. It also presents with the use of non-psychiatric medications, including calcium channel blockers, antibiotics, anti-nausea and anti-vertigo drugs.
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Candida auris is one of the few Candida species that can cause candidiasis in humans. Candidiasis is most often acquired in hospitals by patients with weakened immune systems. It can cause invasive candidiasis, in which the blood stream (fungemia), the central nervous system, kidneys, liver, bones, muscles, joints, spleen, or eyes are invaded. It usually presents with other co-morbidities such as diabetes, sepsis, lung diseases, and kidney diseases.
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The age at which child presents with KDSS may vary from new born to as late as 11 years of age. This disease is very rare as only less than 10% of children with hypothyroid myopathy develops this condition. Along with features of hypothyroidism the main additional feature is muscle hypertrophy.It can happen in any muscle of the limbs, but commonly affects the proximal muscles giving the typical Hercules appearance.
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The Port Harcourt Carnival bears a certain uniqueness as it combines two carnivals - a purely cultural carnival and a contemporary Caribbean style carnival- in one. It also features musical performances from both local and international artists. This gives it an edge over all other regional and continental carnivals, and presents with the principal advantage which must be consummately exploited. The Government of Rivers State recognizes Carniriv as its biggest tourism export.
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While BPH rarely causes sudden urinary retention, the condition can become acute in the presence of certain medications (blood pressure pills, anti histamines, antiparkinson medications), after spinal anaesthesia or stroke. In young males, the most common cause of urinary retention is infection of the prostate (acute prostatitis). The infection is acquired during sexual intercourse and presents with low back pain, penile discharge, low grade fever and an inability to pass urine.
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PDPH typically occurs hours to days after puncture and presents with symptoms such as headache (which is mostly bi-frontal or occipital) and nausea that typically worsen when the patient assumes an upright posture. The headache usually occurs 24–48 hours after puncture but may occur as many as 12 days after. It usually resolves within a few days but has been rarely documented to take much longer.
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The Pai Syndrome is a rare subtype of frontonasal dysplasia. It is a triad of developmental defects of the face, comprising midline cleft of the upper lip, nasal and facial skin polyps and central nervous system lipomas. When all the cases are compared, a difference in severity of the midline cleft of the upper lip can be seen. The mild form presents with just a gap between the upper teeth.
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Convulsive status epilepticus presents with a regular pattern of contraction and extension of the arms and legs. Epilepsia partialis continua is a variant involving hour-, day-, or even week-long jerking. It is a consequence of vascular disease, tumors, or encephalitis, and is drug-resistant. Generalized myoclonus is commonly seen in comatose people following CPR and is seen by some as an indication of catastrophic damage to the neocortex.
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A Hypotensive transfusion reaction or HTR is a rare condition that presents with low blood pressure associated with administration of blood products. The low blood pressure quickly resolves when the transfusion is stopped. HTRs are caused by the production of bradykinin produced through Factor XII activation by negatively charged surfaces such as filters. When mechanisms for the degradation of bradykinin are impaired, the peptide builds up and causes hypotension.
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A manifesting carrier usually has no noticeable problems at birth; symptoms show up later in life. In X-inactivation, the female (who would otherwise be a carrier, without any symptoms), actually presents with full-blown X-linked MTM. Thus, she congenitally presents (is born with) MTM. Thus, although MTM1 mutations most commonly cause problems in boys, these mutations can also cause clinical myopathy in girls, for the reasons noted above.
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Classic phosphofructokinase deficiency is the most common type of this disorder. This type presents with exercise-induced muscle cramps and weakness (sometimes rhabdomyolysis), myoglobinuria, as well as with haemolytic anaemia causing dark urine a few hours later. Hyperuricemia is common, due to the kidneys' inability to process uric acid following damage resulting from processing myoglobin. Nausea and vomiting following strenuous exercise is another common indicator of classic PFK deficiency.
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Primary mediastinal large B-cell lymphoma (PMBL), also termed primary mediastinal (thymic) large B-cell lymphoma, is a DLBCL in which neoplastic B-cells infiltrates are commonly located in sclerotic/fibrous tissues of the thymus and mediastinal lymph nodes. The disease represents 6–10% of all DLBCL cases, presents with early stage disease in ~80% of cases, and has an overall survival rate at 5 years of 75-85%.
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Mallory–Weiss syndrome or gastro-esophageal laceration syndrome refers to bleeding from a laceration in the mucosa at the junction of the stomach and esophagus. This is usually caused by severe vomiting because of alcoholism or bulimia, but can be caused by any condition which causes violent vomiting and retching such as food poisoning. The syndrome presents with hematemesis. The laceration is sometimes referred to as a Mallory-Weiss tear.
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Unfortunately, he did not make it to the Top 5 as the final member of BoybandPH. He made his acting debut in 2017 via TV5's Wattpad Presents with Louise delos Reyes. Later, he joined La Luna Sangre considered as his first break playing the role of Jake Arguelles. His character was set to become a third person in the love triangle between him, Kathryn Bernardo and Daniel Padilla.
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Congestive heart failure frequently presents with shortness of breath with exertion, orthopnea, and paroxysmal nocturnal dyspnea. It affects between 1–2% of the general United States population and occurs in 10% of those over 65 years old. Risk factors for acute decompensation include high dietary salt intake, medication noncompliance, cardiac ischemia, abnormal heart rhythms, kidney failure, pulmonary emboli, hypertension, and infections. Treatment efforts are directed towards decreasing lung congestion.
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People with chronic obstructive pulmonary disease (COPD), most commonly emphysema or chronic bronchitis, frequently have chronic shortness of breath and a chronic productive cough. An acute exacerbation presents with increased shortness of breath and sputum production. COPD is a risk factor for pneumonia; thus this condition should be ruled out. In an acute exacerbation treatment is with a combination of anticholinergics, beta2-adrenoceptor agonists, steroids and possibly positive pressure ventilation.
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Conversion disorder presents with symptoms that typically resemble a neurological disorder such as stroke, multiple sclerosis, epilepsy or hypokalemic periodic paralysis. The neurologist must carefully exclude neurological disease, through examination and appropriate investigations. However, it is not uncommon for patients with neurological disease to also have conversion disorder. In excluding neurological disease, the neurologist has traditionally relied partly on the presence of positive signs of conversion disorder, i.e.
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Recent review studies suggest that the IGDS9-SF presents with robust empirical and clinical evidence and is an effective tool to assess IGD. Moreover, the scale was adapted in several languages as Spanish, Chinese, Czech, German, and so many more. On 3 June 2019, a screening tool for Gaming Disorder, specifically as defined by the World Health Organization, called the "Gaming Disorder Test" was published in a journal article.
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In 2000, he moved to Berlin. Curry has released three full-length albums, Parts Water in 2001, Tainted Lunch (released on Stefan Behnke's ~scape label) in 2005, and Pigeon Funk Presents!!! with Sutekh and Kit Clayton. Parts Water was described by CMJ New Music Monthly as "a perfect headphone record", including what reviewer Tim Haslett called "possibly the first attempts by a techno artist to write pop tunes".
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Ehrlichia ewingii is a human pathogen which results in a serious infection if not treated in a timely manner. Ehrlichiosis, the disease caused by E. ewingii and E. chaffeensis, presents with fever, headache, fatigue, and muscle aches. These symptoms are extremely unspecific which makes the infections difficult to diagnose. Doxycycline is effective when administered early in the infection, but despite this, the estimated fatality rate is still 1.8%.
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In the case of a resistant or reoccurring lesion, chemotherapy has been used as a treatment. Ocular JXG is usually unilateral and presents with a tumor, a red eye with signs of uveitis, unilateral glaucoma, spontaneous hyphema or heterochromia iridis. Diagnosing and treating the patient as early as possible contributes to the most positive visual outcome. Histiocytic disorders like JXG are identified by the cells that make them up.
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Angiolymphoid hyperplasia with eosinophilia (also known as: "Epithelioid hemangioma," "Histiocytoid hemangioma," "Inflammatory angiomatous nodule," "Intravenous atypical vascular proliferation," "Papular angioplasia," "Inflammatory arteriovenous hemangioma," and "Pseudopyogenic granuloma") usually presents with pink to red-brown, dome-shaped, dermal papules or nodules of the head or neck, especially about the ears and on the scalp.James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. .
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During the holidays, she invited staff members and their families to Thanksgiving dinner and opened presents with them on Christmas morning. The White House telegraph operator and secretaries were included in the Thanksgiving group. The group was so large it took three turkeys and a roast pig to feed them all. Lucy was generally kind towards the White House staff, she also allowed White House servants to take time off to attend school.
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Thoracic outlet syndrome (TOS) is a condition in which there is compression of the nerves, arteries, or veins in the passageway from the lower neck to the armpit. There are three main types: neurogenic, venous, and arterial. The neurogenic type is the most common and presents with pain, weakness, and occasionally loss of muscle at the base of the thumb. The venous type results in swelling, pain, and possibly a bluish coloration of the arm.
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TMoA is classified as a non-fluent aphasia that is characterized by a significantly reduced output of speech, but good auditory comprehension. Auditory comprehension skills remain intact because the arcuate fasciculus and Wernicke's area are not impaired. Individuals with TMoA also exhibit good repetition skills and can repeat long, complex phrases effortlessly and without error. However, spontaneous speech often presents with paraphasias (a wide category of speech errors that are caused by aphasia).
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Cornelia de Lange syndrome (CdLS) is a rare genetic disorder that presents with variable clinical abnormalities including dysmorphic features, severe growth retardation, global developmental delay, and intellectual disability. The frequency varies from 1:10 000 to 1:30 000 live births without differences between ethnic groups. SMC1A is one of five genes that have been implicated in CdLS. Pathogenic variants in SMC1A, missense and small in frame deletions, are associated with CdLS.
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Primary small intestinal MZL, also termed primary small intestinal MALT lymphoma, commonly presents with colicky abdominal pain, diarrhea, and in cases of advanced disease signs and symptoms of malabsorption (e.g. weight loss, malnutrition, and anemia), small bowel obstruction, ascites (i.e. fluid in the abdominal cavity), and/or enlargements of lymph nodes, spleen, and/or liver. While generally a progressive disease, patients with early stage primary small intestinal MZL may have spontaneous and complete remissions.
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Tibial plateau fractures typically presents with knee effusion, swelling of the knee soft tissues and inability to bear weight. The knee may be deformed due to displacement and/or fragmentation of the tibia which leads to loss of its normal structural appearance. Blood in the soft tissues and knee joint (hemarthrosis) may lead to bruising and a doughy feel of the knee joint. Due to the tibial plateau's proximity to important vascular (i.e.
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Primary lateral sclerosis (PLS) usually presents with gradual-onset, progressive, lower-extremity stiffness and pain due to muscle spasticity. Onset is often asymmetrical. Although the muscles do not appear to atrophy as in ALS (at least initially), the disabling aspect of PLS is muscle spasticity and cramping, and intense pain when those muscles are stretched, resulting in joint immobility. A normal walking stride may become a tiny step shuffle with related instability and falling.
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Subphrenic abscess is a disease characterized by an accumulation of infected fluid between the diaphragm, liver, and spleen. This abscess develops after surgical operations like splenectomy. Presents with cough, increased respiratory rate with shallow respiration, diminished or absent breath sounds, hiccups, dullness in percussion, tenderness over the 8th–11th ribs, fever, chills, anorexia and shoulder tip pain on the affected side. Lack of treatment or misdiagnosis could quickly lead to sepsis, septic shock, and death.
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Stage 2 is known as the Early Disseminated stage and occurs weeks - months after infection if left untreated. The bacteria spreads via the blood through the body to affect the organs. It often presents with general symptoms such as fever, chills, fatigue, and lymphadenopathy as well as the organ-specific symptoms. It can affect the heart causing myocarditis and arrythmias such as Atrioventricular blocks (which if significant enough may require the insertion of a pacemaker).
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Chronic bacterial prostatitis is a relatively rare condition that usually presents with an intermittent UTI-type picture. It is defined as recurrent urinary tract infections in men originating from a chronic infection in the prostate. Symptoms may be completely absent until there is also bladder infection, and the most troublesome problem is usually recurrent cystitis. Chronic bacterial prostatitis occurs in less than 5% of patients with prostate-related non-BPH lower urinary tract symptoms (LUTS).
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Known as F- cells they are present in a small proportion of overall RBCs. Homozygous Hb Lepore is similar to beta-thalassemia major; however, the clinical course is variable. Patients with this condition typically present with severe anemia during the first two years of life. The heterozygote form is mildly anemic (Hb 11–13 g/dl) but presents with a significant hypochromia (deficiency of hemoglobin in the red blood cells) and microcytosis.
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Under electron microscopy, subendothelial deposits are noted, and some mesangial changes may be present. Clinically, haematuria and proteinuria are present, frequently with nephrotic syndrome, hypertension, hypocomplementemia, elevated anti-dsDNA titres and elevated serum creatinine. Class V disease (membranous glomerulonephritis) is characterized by diffuse thickening of the glomerular capillary wall (segmentally or globally), with diffuse membrane thickening, and subepithelial deposits seen under the electron microscope. Clinically, stage V presents with signs of nephrotic syndrome.
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The damaged structure then produces the symptoms the patient presents with. Ototoxicity in the cochlea may cause hearing loss of the high-frequency pitch ranges or complete deafness, or losses at points between. It may present with bilaterally symmetrical symptoms, or asymmetrically, with one ear developing the condition after the other or not at all. The time frames for progress of the disease vary greatly and symptoms of hearing loss may be temporary or permanent.
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Rosenberg diagrams this sequence in part like this: Observations > Feelings > Needs > Requests where identifying needs is most significant to the process. People also talk about the needs of a community or organisation. Such needs might include demand for a particular type of business, for a certain government program or entity, or for individuals with particular skills. This is an example of metonymy in language and presents with the logical problem of reification.
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Cases of the disease not associated with mediastinal germ cell tumors occur in adults who as a group have older median age centering around those 50–70 years old. The disorder is far more fulminant than non-DS-AMKL and DS-AMKL and generally presents with more serious hematological symptoms (e.g. anemia- related) and a much higher incidence of extramedullary manifestations (e.g. organ enlargement, leukemia cutis) than seen in the other two forms of AMKL.
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It is specific for the phosphate groups of DNA and attaches itself to regions of DNA where there are high amounts of adenine-thymine bonding. Giemsa stain is used in Giemsa banding, commonly called G-banding, to stain chromosomes and often used to create a karyogram (chromosome map). It can identify chromosomal aberrations such as translocations and rearrangements. It stains the trophozoite Trichomonas vaginalis, which presents with greenish discharge and motile cells on wet prep.
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These include: peripheral neuropathy, amyotrophy, ataxia, intellectual disability, ichthyosis, epilepsy, optic neuropathy, dementia, deafness, or problems with speech, swallowing or breathing. Anita Harding classified the HSP in a pure and complicated form. Pure HSP presents with spasticity in the lower limbs, associated with neurogenic bladder disturbance as well as lack of vibration sensitivity (pallhypesthesia). On the other hand, HSP is classified as complex when lower limb spasticity is combined with any additional neurological symptom.
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Sinus arrhythmia is a commonly encountered variation of normal sinus rhythm. Sinus arrhythmia characteristically presents with an irregular rate in which the variation in the R-R interval is greater than 0.12 seconds. Additionally, P waves are typically mono-form and in a pattern consistent with atrial activation originating from the sinus node. During respiration, the intermittent vagus nerve activation occurs, which results in beat to beat variations in the resting heart rate.
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Neu- Laxova syndrome presents with severe malformations leading to prenatal or neonatal death. Typically, NLS involves characteristic facial features, decreased fetal movements and skin abnormalities. Fetuses or newborns with Neu–Laxova syndrome have typical facial characteristics which include proptosis (bulging eyes) with eyelid malformations, nose malformations, round and gaping mouth, micrognathia (small jaw) and low set or malformed ears. Additional facial malformations may be present, such as cleft lip or cleft palate.
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Longer numbers become stories. The long number 27636339, for example, could be chunked into 2763 6339 and then converted into BGSC SCCN. If the memorizer has also associated Santa Claus delivering presents with SC, then the chunk 2763 would represent Bill Gates delivering presents while 6339 would represent Santa Claus performing a roundhouse kick. The remembered story, therefore, could be that Bill Gates delivered presents and then got roundhouse kicked by Santa Claus.
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Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease, occurring in 1:500 individuals in the general population. It is estimated that there are 600,000 individuals in the United States with hypertrophic cardiomyopathy. The most common variant of HCM presents with left ventricular (LV) intracavitary obstruction due to systolic anterior motion of the mitral valve, and mitral-septal contact, diagnosed readily with echocardiography. Pharmacologic treatment with negative inotropic drugs is first-line therapy.
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However, other organs can be affected: strokes, heart attacks, and cardiovascular disease are common additional symptoms. Approximately 40% of VHL disease presents with CNS hemangioblastomas and they are present in around 60-80%. Spinal hemangioblastomas are found in 13-59% of VHL disease and are specific because 80% are found in VHL disease. Although all of these tumours are common in VHL disease, around half of cases present with only one tumour type.
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Pitted keratolysis typically presents with white discoloration of the skin and numerous discrete, "punched-out" pitted lesions or erosions, usually located on the soles of the feet. The pits are typically 1-7 millimeters in diameter. These circular and shallow pits are characteristic of pitted keratolysis, and often overlap to produce larger areas of erosion. The appearance of this condition’s characteristic lesions becomes more pronounced when the affected area is wet or submerged in water.
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Each patient presents with different malocclusion and will need different amount of expansion. It is a general rule to expand the maxilla to a point where the lingual cusp of maxillary molar teeth touch the buccal cusp of mandibular molar teeth. Studies done decades ago by Krebs (1964), Stockfisch (1969) and Linder Aronson (1979) showed that about one-third to one-half of the expansion was lost before the expansion was eventually stabilized.
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Acute tubular necrosis (ATN) is a medical condition involving the death of tubular epithelial cells that form the renal tubules of the kidneys. ATN presents with acute kidney injury (AKI) and is one of the most common causes of AKI. Common causes of ATN include low blood pressure and use of nephrotoxic drugs. The presence of "muddy brown casts" of epithelial cells found in the urine during urinalysis is pathognomonic for ATN.
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As Santa replaces the Halloween-style presents with genuine ones, the townspeople of Halloween Town celebrate Jack's survival and return. Santa then visits Halloween Town and brings them a snowfall for the residents to play with, which in a way, fulfills Jack's original dream. As he flies away, Santa shouts out, "Happy Halloween!" and Jack replies by shouting, "Merry Christmas!". In the graveyard, Jack and Sally declare their love for each other.
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Congenital tracheomalacia often improves without specific intervention; when required, interventions may include beta agonists and muscarinic agonists, which enhance the tone of the smooth muscle surrounding the trachea; positive pressure ventilation, or surgery, which may include the placement of a stent, or the removal of the affected part of the trachea. In dogs, particularly miniature dogs and toy dogs, tracheomalacia, as well as bronchomalacia, can lead to tracheal collapse, which often presents with a honking goose-like cough.
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The programme begins on BT Sport 1 after the final whistle of the live lunchtime game has been shown. Most weeks, Mark Pougatch presents with Jules Breach providing EFL and social media updates. Occasionally, Breach presents alongside Jeff Brazier, on weeks where Mark is not present such as the Rugby World Cup. After 15–20 minutes of build up, the 3pm kickoffs are watched on monitors in the BT Sport studio by a variety of pundits each week.
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The two boys that are chosen are Peter, the poor boy, and the Prince. While the Prince hates the work in the garden and is always being punished, Peter is enamored and loves tending to and watching the presents he planted grow. One day, nearly at Christmas time, the Prince escapes from the convent, and unsuccessfully tries to bring a sack of presents with him. This same day, Peter's younger, disabled sister sneaks into the garden.
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The middle cerebral artery is most often affected. Parenchymal syphilis occurs years to decades after initial infection. It presents with the constellation of symptoms known as tabes dorsalis, because of a degenerative process of the posterior columns of the spinal cord. The constellation includes Argyll Robertson pupil, ataxic wide- based gait, paresthesias, bowel or bladder incontinence, loss of position and vibratory sense, loss of deep pain and temperature sensation, acute episodic gastrointestinal pain, Charcot joints, and general paresis.
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Adams believes that House is losing his observational skills, but the rest of the team believe that nothing is wrong at all. The team believe that he was faking to get out of military prison, but when questioned, the man explains his actions. He also presents with 2 more symptoms, bruising on his abdomen and his legs. House and the team come up with various procedures and decide to ultrasound his belly to find any obstructions.
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Deodorant, talcum powder or lotion may show up on the X-ray as calcium spots, so women are discouraged from applying them on the day of their exam. There are two types of mammogram studies: screening mammograms and diagnostic mammograms. Screening mammograms, consisting of four standard X-ray images, are performed yearly on patients who presents with no symptoms. Diagnostic mammograms are reserved for patients with breast symptoms, changes, or abnormal findings seen on their screening mammograms.
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Intrahepatic cholestasis of pregnancy (ICP), also known as obstetric cholestasis, cholestasis of pregnancy, jaundice of pregnancy, and prurigo gravidarum, is a medical condition in which cholestasis occurs during pregnancy. It typically presents with itching and can lead to complications for both mother and baby. Pruritus (itching) is a common symptom of pregnancy, affecting around 20% of women. The majority of times, itching is a minor annoyance caused by changes to the skin, especially that of the abdomen.
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According to the diaries of Levenstern, he shoot himself in the face and badly disfigured it. According to Ratmanov and Levenstern, while being on the Marquesas Islands, Golovachev took the Rezanov's side and was counting on a career in the RAC. However, as a result, he quarrelled with the officers who saw in him the ambassador's henchman. Probably, he thought about a suicide while being in China, because he made presents with his monogram for many officers.
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In Europe two hantaviruses – Puumala and Dobrava- Belgrade viruses – are known to cause hemorrhagic fever with renal syndrome. Puumala usually causes a generally mild disease, nephropathia epidemica, which typically presents with fever, headache, gastrointestinal symptoms, impaired renal function and blurred vision. Dobrava infections are similar, except that they often also have hemorrhagic complications. Puumala virus is carried by its rodent host, the bank vole (Clethrionomys glareolus), and is present throughout most of Europe, except for the Mediterranean region.
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The alpha-3 subunit (COL4A3) of collagen IV is thought to be the antigen implicated in Goodpasture syndrome, wherein the immune system attacks the basement membranes of the glomeruli and the alveoli upon the antigenic site on the alpha-3 subunit becomes unsequestered due to environmental exposures. Goodpasture syndrome presents with nephritic syndrome and hemoptysis. Microscopic evaluation of biopsied renal tissue will reveal linear deposits of Immunoglobulin G by immunofluorescence. This is classically in young adult males.
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Each wing is covered in multi-layered scales, which are responsible for the coloration of the wings. The wing colors vary with viewing angle, a phenomenon referred to as structural color. In the female, the dorsal side is more camouflaged while the male presents with a vibrant blue. In the male, the outer layer of the cover scales are long and narrow (250 um x 50 um), 2 um apart, and parallel to the wing plane.
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He worked on the children's Saturday morning show, TMi, on BBC Two, which started on 17 September 2006. The series finished on 7 February 2007. Sam returned to television at the beginning of the Easter holidays 2007 in a show called Do Something Different which he presents with Rhodes and Ayesha Asantewaa to attempt to get 1 million children to "try something new". Sam (along with Mark Rhodes) is the presenter of TMi Friday on the CBBC Channel.
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This disease is most commonly caused by an appendiceal primary cancer (cancer of the appendix); mucinous tumors of the ovary have also been implicated, although in most cases ovarian involvement is favored to be a metastasis from an appendiceal or other gastrointestinal source. Disease is typically classified as low- or high-grade (with signet ring cells). When disease presents with low-grade histologic features the cancer rarely spreads through the lymphatic system or through the bloodstream.
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Ventricular tachycardia, which describes a heart rate of over 100 beats per minute with at least three irregular heartbeats as a sequence of consecutive premature beats, can degenerate into ventricular fibrillation, which is rapidly fatal without cardiopulmonary resuscitation (CPR) and defibrillation. Long QT syndrome can cause syncope when it sets off ventricular tachycardia or torsades de pointes. The degree of QT prolongation determines the risk of syncope. Brugada syndrome also commonly presents with syncope secondary to arrhythmia.
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Spontaneous rectus sheath hematoma arises from rupture of the epigastric vessels. The patient usually presents with a sudden well-localized abdominal pain associated with a tender nonpulsatile abdominal mass, usually in the lower abdomen. There is frequently a plausible precipitating factor such as local trauma, a bout of coughing or anticoagulant therapy. The diagnosis can be confirmed on ultrasound examination and a conservative approach to treatment can be adopted provided that the hematoma does not enlarge.
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Junctional epidermolysis bullosa is an inherited disease affecting laminin and collagen. This disease is characterised by blister formation within the lamina lucida of the basement membrane zone and is inherited in an autosomal recessive manner. It also presents with blisters at the site of friction, especially on the hands and feet, and has variants that can occur in children and adults. Less than one person per million people is estimated to have this form of epidemolysis bullosa.
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Neurogenic claudication can occur in cases of severe lumbar spinal stenosis and presents with symptoms of pain in the lower back, buttock or leg that is worsened by standing and relieved by sitting. Vertebral compression fractures occurs in 4 percent of patients presenting to primary care with low back pain. Risk factors include age, female gender, history of osteoporosis, and chronic glucocorticoid use. Fractures can occur due to trauma but in many cases can be asymptomatic.
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Another possible cause of diarrhea is irritable bowel syndrome (IBS), which usually presents with abdominal discomfort relieved by defecation and unusual stool (diarrhea or constipation) for at least three days a week over the previous three months. Symptoms of diarrhea-predominant IBS can be managed through a combination of dietary changes, soluble fiber supplements and medications such as loperamide or codeine. About 30% of patients with diarrhea-predominant IBS have bile acid malabsorption diagnosed with an abnormal SeHCAT test.
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MHF presents with a high fever 104 °F (~40˚C) and a sudden, severe headache, with accompanying chills, fatigue, nausea, vomiting, diarrhea, pharyngitis, maculopapular rash, abdominal pain, conjunctivitis, & malaise. # Early Organ Phase: Day 5 up to Day 13. Symptoms include prostration, dyspnea, edema, conjunctival injection, viral exanthema, and CNS symptoms, including encephalitis, confusion, delirium, apathy, and aggression. Hemorrhagic symptoms typically occur late and herald the end of the early organ phase, leading either to eventual recovery or worsening & death.
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Another serious complication that can result from lesions above T6 is neurogenic shock, which results from an interruption in output from the sympathetic nervous system responsible for maintaining muscle tone in the blood vessels. Without the sympathetic input, the vessels relax and dilate. Neurogenic shock presents with dangerously low blood pressure, low heart rate, and blood pooling in the limbs—which results in insufficient blood flow to the spinal cord and potentially further damage to it.
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Morvan's syndrome is a rare, life-threatening autoimmune disease named after the nineteenth century French physician Augustin Marie Morvan. "La chorée fibrillaire" was first coined by Morvan in 1890 when describing patients with multiple, irregular contractions of the long muscles, cramping, weakness, pruritus, hyperhidrosis, insomnia, and delirium. It normally presents with a slow insidious onset over months to years. Approximately 90% of cases spontaneously go into remission, while the other 10% of cases lead to death.
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Cornelia de Lange syndrome (CdLS) is a rare genetic disorder that presents with variable clinical abnormalities including dysmorphic features, severe growth retardation, global developmental delay, and intellectual disability. SMC3 is one of five genes that have been implicated in CdLS. In one case report, a novel SMC3 gene duplication was detected in a child with failure to thrive, hypotonia and facial dysmorphic features of CdLS. The same duplication was also observed in the mother, who had milder dysmorphic facies.
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Prognosis of gliomas is given in relation to what grade (as scored by the World Health Organization system) of tumour the patient presents with. Typically, any tumour presenting as above WHO grade I (i.e. a malignant tumour as opposed to a benign tumour) will have a prognosis resulting in eventual death, varying from years (WHO grade II/III) to months (WHO grade IV). Prognosis can also be given based on cellular subtype, which may also impact prognosis.
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Alternatives for people who are seriously allergic to penicillin or infections with methicillin-resistant Staphococcus aureus include doxycycline, clindamycin, and trimethoprim-sulphamethoxazole, although doxycycline should not be used in children under the age of eight years old due to the risk of drug-induced tooth discolouration. When streptococci alone are the cause, penicillin is the drug of choice. When the condition presents with ulcers, valacyclovir, an antiviral, may be given in case a viral infection is causing the ulcer.
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Antinuclear antibodies cause an inflammation in the uterus that does not allow it to be a suitable host for implantation of the embryo. Natural killer cells misinterpret the fetal cells as cancer cells and attack them. An individual that presents with reproductive autoimmune failure syndrome has unexplained infertility, endometriosis, and repetitive miscarriages due to elevated levels of antinuclear antibodies circulating. Both the presence of anti-phospholipids antibodies and antinuclear antibodies have toxic effects on the implantation of embryos.
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Other bacterial causes of neonatal CAP include Listeria monocytogenes and a variety of mycobacteria. CAP-causing viruses may also be transferred from mother to child; herpes simplex virus, the most common, is life-threatening, and adenoviridae, mumps and enterovirus can also cause pneumonia. Another cause of neonatal CAP is Chlamydia trachomatis, which, though acquired at birth, does not cause pneumonia until two to four weeks later. It usually presents with no fever and a characteristic, staccato cough.
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If the tremor of the other hand entrains to the same rhythm, stops, or if the patient has trouble copying a simple movement this may indicate a functional tremor. Functional dystonia usually presents with an inverted ankle posture or clenched fist. Positive features of dissociative or non-epileptic attacks include prolonged motionless unresponsiveness, long duration episodes (>2minutes) and symptoms of dissociation prior to the attack. These signs can be usefully discussed with patients when the diagnosis is being made.
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The carriage and stable structure contains numerous alterations from various periods, from the late 19th century through the 20th. These alterations illustrate its adaptation early on, for use as a residence. A doorway was cut into the wall connecting the attached 1840s cottage residence to the carriage house, so that now they are viewed as one residential building. Jefferis now presents with dominant gable over the entrance door with symmetrical bay windows, a verandah and french doors.
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SCD is often considered a subset of SNAS, but with only skin manifestations. SNAS presents with an array of symptoms ranging from respiratory to generalized skin rash to gastrointestinal symptoms A meta review evaluating SNAS found that 1% of patients sensitized to nickel reacted to the nickel content of a 'normal' diet, and with increasing doses of nickel more individuals reacted SNAS is a multilayered immunologic response demonstrating variance between individuals and doses of nickel exposure.
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Decorticate posturing, with elbows, wrists and fingers flexed, and legs extended and rotated inward Brain herniation frequently presents with abnormal posturing, a characteristic positioning of the limbs indicative of severe brain damage. These patients have a lowered level of consciousness, with Glasgow Coma Scores of three to five. One or both pupils may be dilated and fail to constrict in response to light. Vomiting can also occur due to compression of the vomiting center in the medulla oblongata.
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Heat stroke generally presents with a hyperthermia of greater than in combination with disorientation. There is generally a lack of sweating in classic heatstroke, while sweating is generally present in exertional heatstroke. Before a heat stroke occurs, people show signs of heat exhaustion such as dizziness, mental confusion, headaches, and weakness; if a heat stroke occurs when the person is asleep, symptoms may be harder to notice. However, in exertional heat stroke, the affected person may sweat excessively.
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Chorea gravidarum is a rare type of chorea which presents with involuntary abnormal movement, characterized by abrupt, brief, nonrhythmic, nonrepetitive movement of any limb, often associated with nonpatterned facial grimaces. It is a complication of pregnancy which can be associated with eclampsia and its effects upon the basal ganglia. It is not a causal or pathologically distinct entity but a generic term for chorea of any cause starting during pregnancy. It is associated with history of Sydenham's chorea.
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In 1988 Frederick Forsyth secured a contract with London Weekend Television for six thrillers under the headline name of Frederick Forsyth Presents, with a book to be linked to the series, which came out in 1991 as The Deceiver.Richard Joseph, Richard Joseph's Bestsellers (Summersdale, 1997), p. 222 The first three episodes were filmed, and the launch of the series was fixed for December 1989. In the run-up to that, the producers said they were hoping to attract eight million television viewers.
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Congenital heart defects may not show signs or symptoms until later stages of the child's life and have a delayed diagnosis. Congenital stenosis of the inferior vena cava is asymptomatic in many patients. Adolescent males with the condition have shown to presents with symptoms such as spontaneous lower extremity DVT, leg swelling, leg pain, varices in the lower extremities, hepatic thrombosis and hematochezia. Chylothorax has been observed rarely as a symptom of congenital stenosis of the superior vena cava in infant patients.
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Teaming up with a Spanish undertaker Martin, the pair embark on the hazardous trip to Leila's mountain village of Hansala in the Moroccan countryside. Leila's most fundamental beliefs are challenged, as she must face her family, and their grief, anger and love. Martin meanwhile is surprised by his welcome in the village. Director Chus Gutierrez presents with great sensitivity the opposing viewpoints of her main protagonists, artfully, contrasting the lives of rich and poor, separated by only a few hundred miles.
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In most cases, the prognosis of mucormycosis is poor and has varied mortality rates depending on its form and severity. In the rhinocerebral form, the mortality rate is between 30% and 70%, whereas disseminated mucormycosis presents with the highest mortality rate in an otherwise healthy patient, with a mortality rate of up to 90%. Patients with AIDS have a mortality rate of almost 100%. Possible complications of mucormycosis include the partial loss of neurological function, blindness and clotting of brain or lung vessels.
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It is commonly injured in rear end whiplash injuries, usually resulting from a car crash. This muscle is in front of the spine and is thought by some scientists that it may cause some whiplash patients to have an unnatural lack of curvature in the patients' neck. Acute calcific tendinitis of the longus colli muscle can occur. This presents with acute onset of neck pain, stiffness, dysphagia and odynophagia, and must be distinguished from retropharyngeal abscess and other sinister conditions.
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The Santa Claus character is much older, emerging in US folklore in the early 17th century from the historical figure St. Nicholas of Myra with attributes of various European Christmas traditions, especially from English Father Christmas and Dutch Sinterklaas. The association of Christmas presents with elves has precedents in the first half of the 19th century with the Tomte in Sweden and Nisse in Denmark, and St Nicholas himself is called an elf in A Visit from St. Nicholas (1823).
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In rare cases, however, an abnormality in the thirst mechanism causes gestational DI, and desmopressin should not be used. Diabetes insipidus is also associated with some serious diseases of pregnancy, including pre-eclampsia, HELLP syndrome and acute fatty liver of pregnancy. These cause DI by impairing hepatic clearance of circulating vasopressinase. It is important to consider these diseases if a woman presents with diabetes insipidus in pregnancy, because their treatments require delivery of the baby before the disease will improve.
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This came from the fact that the Afghan civilian furniture was infested with rat lice. House also tells them that typhus presents with psychiatric problems, so he can fight his case by claiming that he had suffered from disease-related mental instability. He rejects this on the basis that it proves that what he did wasn't the right thing and that going to prison allows him to keep his honor. Towards the end of the episode, House confronts Wilson about being the rat.
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Inflammatory Breast Cancer presents with similar effects. Inflammatory Breast Cancer is a rare (only seen in less than 5% of breast cancer diagnosis) yet aggressive form of breast cancer characterized by the swollen, red areas formed on the top of the Breast. The visual effects of Inflammatory Breast Cancer is a result of a blockage of lymph vessels by cancer cells. This type of breast cancer is seen in more commonly diagnosed in younger ages, obese women and African American women.
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Peale's work came under criticism from various mental health experts, theologians, and academics. One general criticism against Peale's book was the lack of verified sources. The Power of Positive Thinking includes many personal anecdotes that the reader has no way of validating. The book includes stories about “a business executive”, “a man, an alcoholic”, “a famous trapeze artist”, “a friend of [Peale’s], a midwestern businessman”, and other unnamed individuals which cannot be verified from the information Peale presents with each anecdote.
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Epididymitis occurs when there is inflammation of the epididymis (a curved structure at the back of the testicle). This condition usually presents with gradual onset of varying degrees of pain, and the scrotum may be red, warm and swollen. It is often accompanied by symptoms of a urinary tract infection, fever, and in over half of cases it presents in combination with orchitis. In those between the ages of 14 to 35 it is usually caused by either gonorrhea or chlamydia.
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Dry beriberi affects the nervous system resulting in numbness of the hands and feet, confusion, trouble moving the legs, and pain. A form with loss of appetite and constipation may also occur. Another type, acute beriberi, is found mostly in babies and presents with loss of appetite, vomiting, lactic acidosis, changes in heart rate, and enlargement of the heart. Risk factors include a diet of mostly white rice, as well as alcoholism, dialysis, chronic diarrhea, and taking high doses of diuretics.
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The patient with meningococcal meningitis typically presents with high fever, nuchal rigidity (stiff neck), Kernig's sign, severe headache, vomiting, purpura, photophobia, and sometimes chills, altered mental status, or seizures. Diarrhea or respiratory symptoms are less common. Petechiae are often also present, but do not always occur, so their absence should not be used against the diagnosis of meningococcal disease. Anyone with symptoms of meningococcal meningitis should receive intravenous antibiotics before the results of lumbar puncture, as delay in treatment worsens the prognosis.
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Brandeis University Unisex public toilets can be a suitable alternative in many cases. A special case presents with choirs and choruses, especially in the tradition of the choir school which uses ensemble and musical discipline to ground academic discipline. Male and female voices are distinctive both solo and in ensemble, and segregated singing has an evolved and established aesthetic. Male voices, unlike female voices, break in early adolescence, and accommodating this break in an educational program is challenging in a coed environment.
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The hemophagocytic syndrome-associated variant of IVBCL is a very rare variant of IVBCL. Its previous name, intravascular large B-cell lymphoma, Asian variant, was recently changed to its current name by the world Health Organization, 2016. Unlike the classical and cutaneous variants, the hemophagocytic syndrome-associated variant presents with the hemophagocytic syndrome. This syndrome is characterized by bone marrow involvement, reduced numbers of circulating blood platelets as well as the reduced levels of other circulating blood cells, and enlarged liver and spleen.
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Characteristic skin hyperpigmentation in Addison's disease Addison's disease refers to primary hypoadrenalism, which is a deficiency in glucocorticoid and mineralocorticoid production by the adrenal gland. In the Western world, Addison's disease is most commonly an autoimmune condition, in which the body produces antibodies against cells of the adrenal cortex. Worldwide, the disease is more frequently caused by infection, especially from tuberculosis. A distinctive feature of Addison's disease is hyperpigmentation of the skin, which presents with other nonspecific symptoms such as fatigue.
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The guys find out that on top of a sprained ankle, Santa has also caught a cold, preventing him from delivering the presents. With Christmas in jeopardy, Barney suggests that Fred should be the one to do it. Loving the idea, Santa uses his magic, giving Fred his suit and turning Barney into a Christmas elf, while also instructing Fred on how to drive the sleigh. After a couple of mishaps, Fred and Barney start delivering the presents around the world.
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However, the academic environment frequently presents with situations where negotiation takes place. For example, many faculty are hired with an expectation that they will conduct research and publish scholarly works. For these faculty, where their research requires equipment, space, and/or funding, negotiation of a "start-up" package is critical for their success and future promotion. Also, department chairs often find themselves in situations, typically involving resource redistribution where they must negotiate with their dean, on behalf of their unit.
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Back pain can be caused by the vertebrae compressing the intervertebral discs. Inflammatory arthritides such as ankylosing spondylitis, psoriatic arthritis, rheumatoid arthritis, and systemic lupus erythematosus can all cause varying levels of joint destruction. Among the inflammatory arthritides, ankylosing spondylitis is most closely associated with back pain due to the inflammatory destruction of the bony components of the spine. Ankylosing spondylitis is common in young men and presents with a range of possible symptoms such as uveitis, psoriasis, and inflammatory bowel disease.
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In February 2010, he presents with Sandrine Corman the first season of the French version of Top Chef. He then presents alone the second season in January 2011, the third season in January 2012, and finally the fourth season in February 2013. In April 2012, Rotenberg hosts on M6 the eighth season of Pékin Express, le passager mystère. During the shooting, he was victim of an accident after losing control of his side-car after being violently hit by a car.
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Myelokathexis is amongst the diseases treated with bone marrow transplantation and cord blood stem cells. WHIM syndrome is a very rare variant of severe congenital neutropenia that presents with warts, hypogammaglobunemia, infections, and myelokathexis. A gain-of-function mutation resulting in a truncated form of CXCR4 is believed to be its cause. The truncated form of the receptor has a 2-fold increase in G-protein coupled intracellular signalling, and this mutation of the receptor can be identified by DNA sequencing.
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Laryngopharyngeal reflux (LPR) is the retrograde flow of gastric contents into the larynx, oropharynx and/or the nasopharynx. LPR causes respiratory symptoms such as cough and wheezing and is often associated with head and neck complaints such as dysphonia, globus pharyngis, and dysphagia. LPR may play a role in other diseases, such as sinusitis, otitis media, and rhinitis, and can be a comorbidity of asthma. While LPR is commonly used interchangeably with gastroesophageal reflux disease (GERD), it presents with a different pathophysiology.
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Medical massage is outcome-based massage, primarily the application of a specific treatment targeted to the specific problem(s) the patient presents with a diagnosis and are administered after a thorough assessment/evaluation by the medical massage therapist with specific outcomes being the basis for treatment. It is also known as clinical massage or treatment massage. There are many massage schools and programs that teach medical massage as a technique. Though medical massage is any massage treatment used to treat specific medical conditions.
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Symptoms relate to impaired brain function in areas supplied by the posterior circulation, as seen in posterior circulation strokes. However, symptoms may be far briefer than those seen in stroke. Vertigo is a relatively common symptom that can result from ischemia to the cerebellum, medulla or (rarely) the internal auditory artery which supplies the vestibular system of the inner ear. While vertigo is a common feature of VBI or posterior circulation stroke, VBI only rarely presents with vertigo alone (without other neurological signs).
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The Ashiqa states that a mother Kamala Devi asked Alauddin to snatch her young daughter from her biological father. It goes on to claim that Karna not only readily agreed to this demand, but also decided to send some presents with her to Delhi. These claims, which imply that the Vaghelas had no sense of honour and chastity, seem absurd. Even Bada'uni, who placed a high value on the historicity of Ashiqa, chose to ignore these claims in his writings.
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While it should be considered in a differential, other causes should be considered as well. Cerebral salt wasting syndrome (CSWS) also presents with hyponatremia, there are signs of dehydration for which reason the management is diametrically opposed to SIADH. Importantly CSWS can be associated with subarachnoid hemorrhage (SAH) which may require fluid supplementation rather than restriction to prevent brain damage. Most cases of hyponatremia in children are caused by appropriate secretion of antidiuretic hormone rather than SIADH or another cause.
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Hypermetabolism is defined as an elevated resting energy expenditure (REE) > 110% of predicted REE. Hypermetabolism is accompanied by a variety of internal and external symptoms, most notably extreme weight loss, and can also be a symptom in itself. This state of increased metabolic activity can signal underlying issues, especially hyperthyroidism. Patients with Fatal familial insomnia, an extremely rare and strictly hereditary disorder, also presents with hypermetabolism; however, this universally fatal disorder is exceedingly rare, with only a few known cases worldwide.
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Vitamin K deficiency bleeding (VKDB) of the newborn, previously known as haemorrhagic disease of the newborn, is a rare form of bleeding disorder that affects newborns and young infants due to low stores of vitamin K at birth. It commonly presents with intracranial haemorrhage with the risk of brain damage or death. Newborn infants have low stores of vitamin K, and human breast milk has low concentrations of the vitamin. This combination can lead to vitamin K deficiency and later onset bleeding.
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A modified form of the alpha-synuclein protein within affected neurons may cause MSA. About 55% of MSA cases occur in men, with those affected first showing symptoms at the age of 50–60 years. MSA often presents with some of the same symptoms as Parkinson's disease. However, those with MSA generally show little response to the dopamine medications used to treat Parkinson's disease, and only about 9% of MSA patients with tremor had a true parkinsonian pill-rolling tremor.
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Atherosclerosis narrows blood vessels in the brain, resulting in decreased cerebral perfusion. Other risk factors that contribute to stroke include smoking and diabetes. Narrowed cerebral arteries can lead to ischemic stroke, but continually elevated blood pressure can also cause tearing of vessels, leading to a hemorrhagic stroke. A stroke usually presents with an abrupt onset of a neurologic deficit – such as hemiplegia (one-sided weakness), numbness, aphasia (language impairment), or ataxia (loss of coordination) – attributable to a focal vascular lesion.
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Isosthenuria may be seen in disease states as chronic and acute kidney failure in which the kidneys lack the ability to concentrate or dilute the urine and so the initial filtrate of the blood remains unchanged despite the need to conserve or excrete water based on the body's hydration status.De Mais, Daniel. ASCP Quick Compendium of Clinical Pathology, 2nd Ed. ASCP Press, Chicago, 2009. Sickle- cell trait, the heterozygous form of sickle-cell disease, presents with a normal hematological picture but is associated with hyposthenuria.
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Subacromial bursitis often presents with a constellation of symptoms called impingement syndrome. Pain along the front and side of the shoulder is the most common symptom and may cause weakness and stiffness. If the pain resolves and weakness persists other causes should be evaluated such as a tear of the rotator cuff or a neurological problem arising from the neck or entrapment of the suprascapular nerve. The onset of pain may be sudden or gradual and may or may not be related to trauma.
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Mr. Blackwell was a pioneer in television fashion and had been a fixture in the medium throughout his career as a designer and critic. Most recently, he appeared as himself on an episode of the ABC daytime soap, Port Charles. He hosted a daily program on Los Angeles' talk radio powerhouse KABC from 1972–74, moving to KIEV 1975–1981. In 1968 he starred in his own KCOP two-hour color television special, Mr. Blackwell Presents, with Anna Maria Alberghetti, Nick Adams and Rose Marie.
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Later in life, these individuals may present with photosensitivity similar to that found in cutaneous porphyrias. Biochemically, harderoporphyria presents with a distinct pattern of increased harderoporphyrin (2-vinyl-4,6,7-tripropionic acid porphyrin) in urine and particularly in feces, a metabolite that is not seen in significant quantities in any other porphyria. Enzyme tests show markedly reduced activity of coproporphyrinogen oxidase, compared to both unaffected individuals and those affected with hereditary coproporphyria, consistent with recessive inheritance. Harderoporphyria is a rare condition, with less than 10 cases reported worldwide.
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The presence of glucagonoma syndrome, the symptoms that accompany the pancreatic tumor, as well as elevated levels of glucagon in the blood, are what is used to diagnose glucagonoma. When a person presents with a blood glucagon concentration greater than 500 mg/mL along with the glucagonoma syndrome, a diagnosis can be established. It is important to note that not all cases of hyperglucagonemia will lead to a diagnosis of glucagonoma. Elevated blood levels of glucagon are associated with other disorders like pancreatitis and kidney failure.
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Periampullary cancer is a cancer that forms near the ampulla of Vater, an enlargement of the ducts from the liver and pancreas where they join and enter the small intestine. Quoted material is in the public domain. It consists of: # ampullary tumour from ampulla of Vater # cancer of lower common bile duct # duodenal cancer adjacent to ampulla # carcinoma head of pancreas It presents with painless jaundice which may have waxing and waning nature because at times the sloughing of the tumor tissue relieves the obstruction partially.
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It's a glory. . . See it with your best friend." In his review for Cut Print Film, Josh Oakley awarded the film a perfect "10/10", calling it "one of the best films of the year", and stating "The End of the Tour presents, with ample evidence, Wallace as a figure who could never fill the holes of loneliness with the spackle of acclaim." In his review for the Chicago Sun-Times, Richard Roeper awarded the film four out of four stars, calling it "brilliant. . .
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Mole has extensively investigated the lysosomal disease Batten disease, writing a textbook on the subject and setting up a mutation database and on-line resource web site for patients and their families. Batten disease is characterised by the accumulation of autofluorescent material in lysosomes and presents with visual failure, seizures, cognitive impairment and decline in motor abilities. Mole has contributed to the identification and characterization of thirteen genes that cause Batten disease. Treatments for the majority of these diseases exist only as palliative care.
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A hand imitating an ulnar claw. The metacarpophalangeal joints of the 4th and 5th fingers are extended and the Interphalangeal joints of the same fingers are flexed. An ulnar claw, also known as claw hand, or spinster's claw is a deformity or an abnormal attitude of the hand that develops due to ulnar nerve damage causing paralysis of the lumbricals. A claw hand presents with a hyperextension at the metacarpophalangeal joints and flexion at the proximal and distal interphalangeal joints of the 4th and 5th fingers.
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Lyme disease, caused by the spirochete Borrelia burgdorferi, is a tick-borne illness with both peripheral and central neurological manifestations. The first stage of Lyme disease frequently presents with a pathognomonic "bull's eye" rash, erythema migrans, as well as fever, malaise, and arthralgias. Roughly 15% of untreated patients will then develop neurological manifestations, classically characterized by cranial neuropathy, radiculoneuritis, and a lymphocytic meningitis. The nerve inflammation seen in neurological lyme disease is associated with a lymphoctyic infiltrate without evidence of direct infection of peripheral nerves.
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Pat Hitchcock with her daughter Terry and husband Joseph O'Connell, Alma Reville, Mary Alma O'Connell, Alfred Hitchcock (clockwise from top left), c. 1955–1956 From 1955 to 1965, Hitchcock was the host of the television series Alfred Hitchcock Presents. With his droll delivery, gallows humour and iconic image, the series made Hitchcock a celebrity. The title-sequence of the show pictured a minimalist caricature of his profile (he drew it himself; it is composed of only nine strokes), which his real silhouette then filled.
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Muscle stiffness may also be present; if muscle weakness is not also present, and cramps are more severe, the stiffness may be categorized instead as cramp fasciculation syndrome. Cramp fasciculation is a variant of BFS which presents with muscle pain and exercise intolerance. BFS symptoms are typically not accompanied by severe muscle weakness, and are typically present when the muscle is at rest. Individuals with BFS may have perceived weakness which is the sensation of a fatigued limb, but is not true clinical weakness.
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Several diseases can present with similar signs and symptoms to pneumonia, such as: chronic obstructive pulmonary disease, asthma, pulmonary edema, bronchiectasis, lung cancer, and pulmonary emboli. Unlike pneumonia, asthma and COPD typically present with wheezing, pulmonary edema presents with an abnormal electrocardiogram, cancer and bronchiectasis present with a cough of longer duration, and pulmonary emboli present with acute onset sharp chest pain and shortness of breath. Mild pneumonia should be differentiated from upper respiratory tract infection (URTI). Severe pneumonia should be differentiated from acute heart failure.
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Because these two conditions result from the same genetic changes and can occur in different members of a single family, researchers believe that they may represent a spectrum of overlapping features instead of two distinct syndromes. Mitochondrial complex V deficiency presents with heterogeneous clinical manifestations including neuropathy, ataxia, hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy can present with negligible to extreme hypertrophy, minimal to extensive fibrosis and myocyte disarray, absent to severe left ventricular outflow tract obstruction, and distinct septal contours/morphologies with extremely varying clinical course.
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Conversely, a person with a disability, but who maintains a positive outlook, will be facing to the right, toward a high level of wellness. It is less important where a person is on the Continuum than the direction they are facing. The Illness-Wellness Continuum has been viewed as promoting preventive treatment, which improves wellbeing before an individual presents with signs or symptoms of illness, as well as educating people to be aware of and avoid risk factors, in order to protect against pathology and premature death.
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Frontotemporal lobar degeneration FTLD) is the pathological term for the clinical syndrome of frontotemporal dementia (FTD). FTD differs from the more common Alzheimer's dementia in that memory is relatively well preserved; instead, the disease presents with a more temporal-lobe phenotype. Behavioural variant frontotemporal dementia (bvFTD), progressive non-fluent aphasia (PNFA) and semantic dementia (SD) are the three best-characterised clinical presentations. FUS positive FTLD tends to present clinically as a bvFTD but the correlation between underlying pathology and clinical presentation is not perfect.
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Wound infection by C novyi and many other clostridium species cause gas gangrene Spontaneous infection is mostly associated with predisposing factors of hematologic or colorectal malignancies and with diabetes mellitus, although Gram-negative organisms, including Escherichia coli, may lead to a gas gangrene-like syndrome in diabetic patients. This presents with cellulitis and crepitus, and may be mistaken for gas gangrene. Spontaneous, nontraumatic, or intrinsic infections from a bowel source have been increasingly reported recently. C novyi has been implicated in mortality among injecting illegal drug users.
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Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a diffuse parenchymal lung disease which often presents with symptoms of cough and shortness of breath. The pathological definition published by the World Health Organization is “a generalized proliferation of scattered single cells, small nodules (neuroendocrine bodies), or linear proliferations of pulmonary neuroendocrine (PNE) cells that may be confined to the bronchial and bronchiolar epithelium.” The true prevalence of this disease is not known. To date, just under 200 cases have been reported in the literature.
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The Chopin too, was dazzling and charming at the same time.” 2009 saw Leschenko commence a new position as International Chair in Piano at the Royal Welsh College of Music & Drama in Cardiff, where she began a three-year residency. Polina Leschenko has recorded a début CD for EMI in the series ‘Martha Argerich presents …’ with works by Liszt, Chopin, Kreisler/Rachmaninov, Brahms and Bach/Feinberg. The Gramophone described her as having ‘technical dexterity in abundance, and signs of a major artist in the making’.
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Mina is seen to be a very thorough doctor, treating a man who presents with joint pain as though he has haemorrhagic fever. When Dr. Otis Cole challenges her, she retorts that they are in a hotspot for infectious disease, to which Cole responds that sometimes it is just tennis elbow, from playing tennis. Mina then diagnoses an elderly woman with the common cold, telling her that there is nothing that she can do. The old woman continues to linger at the clinic, much to Mina's annoyance.
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As early as the 1950s, Lliboutry became interested in the Earth's internal structure, and it is remarkable that book chapters and monographs he wrote between 1973 and 2000 are more devoted to geodynamics than glaciology. He notices that the Earth's mantle, even if it deforms a million times slower than glaciers, finally presents with ice a much greater analogy than what can be established between ice and more usual viscous fluids which deform a thousand billion times more quickly.Lliboutry 1999, op. cit., chap. 10.
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The decreased volume of amniotic fluid causes the growing fetus to become compressed by the mother's uterus. This compression can cause many physical deformities of the fetus, most common of which is Potter facies. Lower extremity anomalies are frequent in these cases, which often presents with clubbed feet and/or bowing of the legs..Sirenomelia, or "Mermaid syndrome" (which occurs approximately in 1:45,000 births)Banerjee A, 2003; Indian J Pediatr can also present. In fact, nearly all reported cases of sirenomelia also present with BRA.
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However, transcortical sensory aphasia differs from receptive aphasia in that patients still have intact repetition and exhibit echolalia, or the compulsive repetition of words. Transcortical sensory aphasia cannot be diagnosed through brain imaging techniques such as functional magnetic resonance imaging (fMRI), as the results are often difficult to interpret. Therefore, clinicians rely on language assessments and observations to determine if a patient presents with the characteristics of TSA. Patients diagnosed with TSA have shown partial recovery of speech and comprehension after beginning speech therapy.
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In human herpesvirus 8 associated multicentric Castelman disease (HHV-8-associated MCD), enlarged lymph nodes are present in multiple lymph node regions and infection with human herpesvirus 8 is present. It is less common than unicentric Castleman disease and diagnosed most frequently in patients infected with human immunodeficiency virus (HIV). Compared to UCD and iMCD, HHV-8-associated MCD presents with similar symptoms and clinical findings to iMCD. While UCD is readily treatable with surgery, HHV-8-associated MCD, like iMCD, is treated with medications as surgery is ineffective.
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In early 2013, Stand-Up NY started a new venture called Stand Up NY Labs: a place where free comedy podcasts and videos are produced featuring comedians affiliated with Stand-Up NY. Located directly above the club, the Stand Up NY Labs records podcasts such as "Tuesdays with Stories" with Joe List and Mark Normand, "Charlie Murphy Presents" with Charlie Murphy, "We Know Nothing" with Nikki Glaser, "Race Wars" with Kurt Metzger and Sherrod Small, "My Sexy Podcast" with Sabrina Jalees, and "Invasion of Privacy" with Joe Santagato and Kate Wolff.
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A chest x-ray (radiograph) is often the first imaging test performed when a person presents with cough or chest pain, particularly in the primary care setting. A chest radiograph may detect a lung nodule/mass that is suggestive of cancer, although sensitivity and specificity are limited. CT imaging provides better evaluation of the lungs, with higher sensitivity and specificity for lung cancer compared to chest radiograph (although still significant false positive rate). Computed tomography (CT) that is specifically aimed at evaluating lung cancer includes the chest and the upper abdomen.
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A related condition is luteinizing hormone (LH) insensitivity (termed Leydig cell hypoplasia when it occurs in males), which presents with similar symptoms to those of FSH insensitivity but with the symptoms in the respective sexes reversed (i.e., hypogonadism and sexual infantilism in males and merely problems with fertility in females); however, males also present with feminized or ambiguous genitalia (also known as pseudohermaphroditism), whereas ambiguous genitalia does not occur in females with FSH insensitivity. Despite their similar causes, LH insensitivity is considerably more common in comparison to FSH insensitivity.
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Primary EMZL of the esophagus, also termed MALT lymphoma of the esophagus, is extremely rare with most cases of it being reported from Japan. It presents with symptoms of difficult swallowing and/or sensations of a foreign body in the esophageal area. Endoscopy, endosonography and chest CT scans reveal a solitary esophageal mass of varying size or, more commonly, a linear central indentation or ridge in the esophagus. In a 2017 review, 6 of 18 patients with EMZL of the esophagus had evidence of concurrent Helicobacter pylori infection.
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However, the major sign that would lead a doctor to consider an underlying condition is a dilated aorta or an aortic aneurysm. Sometimes, no heart problems are apparent until the weakening of the connective tissue (cystic medial degeneration) in the ascending aorta causes an aortic aneurysm or aortic dissection, a surgical emergency. An aortic dissection is most often fatal and presents with pain radiating down the back, giving a tearing sensation. Because underlying connective tissue abnormalities cause MFS, the incidence of dehiscence of prosthetic mitral valve is increased.
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The album has been re-released multiple times over the years. The first re-release came when the album was first released on cassette by CD Presents with two more tracks; the 1989 release on CD included the same bonus tracks. In 2000, Lady Butcher released the album on CD with 10 bonus tracks that were recorded live at the Whisky a Go Go in Los Angeles, California, in August 1978. Sometime by 2003, singer Penelope Houston was selling CD-R copies of the album on her website.
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A Frankish mission came to offer Harun friendship in 799. Harun sent various presents with the emissaries on their return to Charlemagne's court, including a clock that Charlemagne and his retinue deemed to be a conjuration because of the sounds it emanated and the tricks it displayed every time an hour ticked.André Clot, Harun al-Rashid and the world of the thousand and one nights, p. 97. Portions of the fictional One Thousand and One Nights are set in Harun's court and some of its stories involve Harun himself.
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The Focus Foundation attempts to increase awareness an X and Y chromosomal variations in order to help children with these disorders. Although all physicians, ancillary health care providers and special educators are taught that genetic abnormalities can impact a child's development, practitioners often receive insufficient information about these disorders, and, therefore, do not often test for X & Y chromosomal variations when a child presents with neurodevelopmental concerns. By promoting awareness of these disorders and associated symptoms, The Focus Foundation hopes to increase early identification, implement interventions, and help families pursue optimal outcomes for their children.
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More recently, researchers have attributed both TTP and HUS to targeted agents, such as targeted cancer therapies, immunotoxins, and anti-VEGF therapy. Bacterial toxins are the primary cause of one category of thrombotic microangiopathy known as HUS or hemolytic uremic syndrome. HUS can be divided into two main categories: Shiga- toxin-associated HUS (STx-HUS), which normally presents with diarrhea, and atypical HUS. The Shiga-toxin inhibits the binding of eEF-1-dependent binding of aminoacyl tRNA to the 60S subunit of the ribosome, thus inhibiting protein synthesis.
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Angioimmunoblastic T cell lymphoma (ATIL) is a systemic malignancy of mature follicular B helper T cells (TFH cells). ATIL is often manifested soon after individuals ingest antibiotics or have an infection or allergic reaction. The disease presents with generalized swelling of lymph nodes, enlarged liver and spleen, skin lesions (rash, or, less commonly, nodules, plaques, purpura, and urticarial), bone marrow involvement, and B symptoms of fever, weight loss, and night sweats. Individuals may also present with arthralgias, arthritis, pleural effusions, ascites, lung lesions, and neurological and gastrointestinal disturbances.
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Testicular torsion usually presents with an acute onset of diffuse testicular pain and tenderness of less than 6 hrs of duration. There is often an absent or decreased cremasteric reflex, the testicle is elevated, and often is horizontal. It occurs annually in about 1 in 4000 males before 25 years of age, is most frequent among adolescents (65% of cases presenting between 12 – 18 years of age), and is rare after 35 years of age. Because it can lead to necrosis within a few hours, it is considered a surgical emergency.
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Sequencing of exons 2, 3, 5, and 10 of this gene detects an estimated 97% of all known mutations. A specific and highly sensitive test for FMF is the "metaraminol provocative test (MPT)", whereby a single 10 mg infusion of metaraminol is administered to the patient. A positive diagnosis is made if the patient presents with a typical, albeit milder, FMF attack within 48 hours. As MPT is more specific than sensitive, it does not identify all cases of FMF, although a positive MPT can be very useful.
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The surviving façade presents with a high degree of architectural integrity and its period detailing is fully compatible with the surviving Victorian imagery of much of the Gloucester Street. While the building is now used as offices, the appearance of the façade maintains a reference to past residential use, and strongly contributes to the aesthetic character of the streetscape. The building has strong visual relationships with adjacent buildings, including the terraces at 32-36 and 38-40 Gloucester Street, which enhance the presentation of its aesthetic character. The item meets this criterion on Local level.
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The surviving façade presents with a high degree of architectural integrity and period detailing fully compatible with the surviving Victorian imagery of much of the Gloucester Street. While the building is now used as offices, the appearance of the façade maintains a reference to past residential use, and strongly contributes to the aesthetic character of the streetscape. The building has strong visual relationships with adjacent buildings, including the terraces at 26-30 and 38-40 Gloucester Street, which enhance the presentation of its aesthetic character. The item meets this criterion on Local level.
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The item does not meet this criterion. The place is important in demonstrating aesthetic characteristics and/or a high degree of creative or technical achievement in New South Wales. The surviving façade presents with a high degree of architectural integrity and its period detailing is fully compatible with the surviving Victorian imagery of much of the Gloucester Street. While the building is now used as offices, the appearance of the façade maintains a reference to past residential use, and strongly contributes to the aesthetic character of the streetscape.
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Color or consistency changes in mucous discharge to yellow, thick, or green are the natural course of viral URTI and not an indication for antibiotics. Group A beta-hemolytic streptococcal pharyngitis/tonsillitis (strep throat) typically presents with a sudden onset of sore throat, pain with swallowing, and fever. Strep throat does not usually cause runny nose, voice changes, or cough. Pain and pressure of the ear caused by a middle-ear infection (otitis media) and the reddening of the eye caused by viral conjunctivitis are often associated with URTIs.
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Reactive arthritis, formerly known as Reiter's syndrome, is a form of inflammatory arthritis that develops in response to an infection in another part of the body (cross-reactivity). Coming into contact with bacteria and developing an infection can trigger the disease. By the time the patient presents with symptoms, often the "trigger" infection has been cured or is in remission in chronic cases, thus making determination of the initial cause difficult. The arthritis often is coupled with other characteristic symptoms; this was previously referred to as Reiter's syndrome, Reiter's disease or Reiter's arthritis.
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Pyruvate dehydrogenase (PDH) deficiency is a congenital degenerative metabolic disease resulting from a mutation of the pyruvate dehydrogenase complex (PDC) located on the X chromosome. While defects have been identified in all 3 enzymes of the complex, the E1-α subunit is predominantly the culprit. Malfunction of the citric acid cycle due to PDH deficiency deprives the body of energy and leads to an abnormal buildup of lactate. PDH deficiency is a common cause of lactic acidosis in newborns and often presents with severe lethargy, poor feeding, tachypnea, and cases of death have occurred.
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Studies have been performed to determine the source of the association between toe walking and cerebral palsy patients. One study suggests that the toe walking—sometimes called an equinus gait—associated with cerebral palsy presents with an abnormally short medial and lateral gastrocnemius and soleus—the primary muscles involved in plantarflexion. A separate study found that the gait could be a compensatory movement due to weakened plantarflexion muscles. The study performed clinical studies to determine that a greater plantarflexion force is required for normal heel-to-toe walking than for toe walking.
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On the wedding day, people would come to congratulate the family early in the morning, whereas in the evening, only those who were invited to the wedding would show up. The guests would bring presents with them for the couple; usually the women would bring pies, and the men, two kilograms of sugar. Among the men, various songs were sung with the cifteli and lute (traditional Albanian instruments) while comedic acts were played on one another. Among the women, two tambourine players would sing rhythmical songs to which women would dance.
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Aspen Santa Fe Ballet (ASFB) is an American contemporary dance company. It comprises eleven classically trained dancers. In addition to its domestic and international performances, the organization has a presentation program called "Aspen Santa Fe Ballet Presents", with summer and winter seasons that brings touring dance companies from around the world to both Aspen and Santa Fe. The Aspen Santa Fe Ballet has two official schools, one in Aspen, one in Santa Fe, and a year-round Mexican Folk Dance outreach program in both Colorado and New Mexico.
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Cyclothymia, a condition of continuous mood fluctuations, is characterized by oscillating experiences of hypomania and depression that fail to meet the diagnostic criteria for either manic or major depressive episodes. These periods are often interspersed with periods of relatively normal (euthymic) functioning. When a patient presents with a history of at least one episode of both hypomania and major depression, each of which meet the diagnostic criteria, bipolar II disorder is diagnosed. In some cases, depressive episodes routinely occur during the fall or winter and hypomanic ones in the spring or summer.
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Those who develop the chronic stages of elephantiasis are usually free from microfilariae (amicrofilaraemic), and often have adverse immunological reactions to the microfilariae, as well as the adult worms. The subcutaneous worms present with rashes, urticarial papules, and arthritis, as well as hyper- and hypopigmentation macules. Onchocerca volvulus manifests itself in the eyes, causing "river blindness" (onchocerciasis), one of the leading causes of blindness in the world. Serous cavity filariasis presents with symptoms similar to subcutaneous filariasis, in addition to abdominal pain, because these worms are also deep-tissue dwellers.
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Ludwig's angina is a form of severe diffuse cellulitis with bilateral involvement, primarily of the submandibular space with the sublingual and submental spaces also being involved. It presents with an acute onset and spreads very rapidly meaning early diagnosis and immediate treatment planning is key to saving lives. The external signs may include bilateral lower facial swelling around the mandible and upper neck. Signs inside the mouth may include elevation of the floor of mouth due to sublingual space involvement and posterior displacement of the tongue, creating the potential for a compromised airway.
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Eventually, Dr. Cuddy sides with Wilson and refuses House any Vicodin, forcing him to detox, and removes him from his team's case: a 15-year-old girl suffering from a collapsed lung and anemia. The patient, Abigail, and her mother, is considered to be suffering from cartilage–hair hypoplasia, a type of dwarfism. Abigail also presents with apparent liver cancer and diabetic ketoacidosis, among other things. House picked up a prescription for pain meds from the hospital pharmacy, supposedly for a patient of Wilson's (it turns out the patient has recently died).
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He played 32 games, with goalkeeper Seymour, half-back Robinson and forward Graham all being ever-presents. With the advent of league football in Bradford, thousands of people came to home games, resulting in the club's end-of-season receipts totalling £3,896. It resulted in a small operating loss from the first season, but donations helped the club record a profit of £39 in their first season in the Football League. Following the end of the season, the club released six players and also sold Guy to Leeds City.
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Retinoblastoma presents with cumulative lifetime incidence rate of one case of retinoblastoma per 18000 to 30000 live births worldwide. A higher incidence is noted in developing countries, which has been attributed to lower socioeconomic status and the presence of human papilloma virus sequences in the retinoblastoma tissue. Almost 80% of children with retinoblastoma are diagnosed before 3 years of age and diagnosis in children above 6 years of age is extremely rare. In the UK, bilateral cases usually present within 14 to 16 months, while diagnosis of unilateral cases peaks between 24 and 30 months.
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In 2009, he returned to acting via Your Song Presents with his partner and fellow singer Nikki Gil. He also released his fifth studio album Groove in the Philippines as well as worldwide digital services later that year. He also hosted a former talent show, Showtime. In 2010, he hosted Pilipinas Got Talent with fellow co-host Luis Manzano and both won as Best Talent Search Program Hosts at the 24th PMPC Star Awards for TV. Since 2011, Crawford has been hosting with Vhong Navarro and other hosts in the weekday variety show It's Showtime.
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The classic presentation is a person who does not move or interact with the world in any way while awake. This type of catatonia presents with waxy flexibility. Waxy flexibility is when someone physically moves part of a catatonic person's body and the person stays in the position even if it is bizarre and otherwise nonfunctional (such as moving a person's arm straight up in the air and the arm staying there). The other type of catatonia is more of an outward presentation of the profoundly agitated state described above.
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The story was also adapted for six television anthology series: on 30 January 1950 for Robert Montgomery Presents with Madeleine Carroll; on 3 November 1952 for Broadway Television Theatre with Sylvia Sidney; on 15 October 1956 for Producers' Showcase (directed by William Wyler), on 2 December 1956 for BBC Sunday-Night Theatre with Celia Johnson. in 1960 for The Somerset Maugham Hour and in 1969 for W. Somerset Maugham (directed by Christopher Morahan). A made-for-TV movie directed by John Erman and starring Lee Remick was made and released in 1982 for ABC.
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In the confusion, Edward and Richard are able to grab and kill a second hunter, and Edward uses the hunter's rifle to kill Titus and the third hunter. Anita stabs Aikensen, and she and Edward leave, allowing Richard to take the now transformed Jason out to hunt, just as the police begin to arrive. The police accept Anita and Edward's story, as well as Edward's identification and claimed identity. In the epilogue, Anita explains that she is continuing to date Richard and Jean- Claude and has exchanged Christmas presents with each of them.
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After the confluence of the GAAP, in the spring 1957, in the group of "Azione Comunista" founded two years earlier by a "dissident" of PCI, Parodi is committed to the side of Arrigo Cervetto against the Maximalism of the group to attest an internationalist position. He presents with Cervetto, at the first conference of the Communist Left November 1957 in Livorno, the "Theses on imperialist development, the duration of the counter and on the development of the class party", that is now expressed in an organic strategic vision of the current Leninist.
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Consequently, the World Health Organization (2017) removed the localized disease from the primary gastrointestinal tract follicular lymphoma category, reclassified it as a distinct disease entity, and termed it duodenal-type follicular lymphoma. DFL is most often an asymptomatic disease that is diagnosed on endoscopic examination of the GI tract conducted for other reasons. Less commonly, it presents with vague abdominal symptoms. In one review of former studies, the lesions in 85% of primary duodenal follicular lymphoma were located not only in the duodenum but also other sites in the intestine (i.e.
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Their route took them across the Orange River to Kuruman, where they met Robert Moffat, who had befriended Mzilikazi and was able to provide Harris with useful information about the ruler. Mzilikazi received Harris' presents with pleasure and the expedition set off confidently for the Magaliesberg toward the south-east. Here they experienced at first hand the struggles of the Voortrekkers against the Matabele. Harris came across his first sable antelope (Hippotragus niger) in the Magaliesberg, and sent a description and specimen of the animal to the Zoological Society of London.
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By applying this methode, a study of 2013 showed that 94% of the patients with the pre-surgery test result "Obstruction" had a successful surgery outcome. In contrast, 70% of the patients with the pre-surgery test result "No Obstruction" had a non-successful surgery outcome. If BPH with obstruction additionally presents with overactive bladder (OAB), which is the case in about 50% of patients, this latter symptom (OAB) persits even post- surgery in about 20% of patients. However, this rate only applies to a period of a few years.
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The addition of weight loss, appetite loss, vomiting, polyuria, and polydipsia to the aforementioned symptoms may indicate that OFC is the result of parathyroid carcinoma. Parathyroid carcinoma, an uncommon cancer of the parathyroid glands, is generally indicated by serum calcium levels higher than usual, even in comparison to the high serum calcium levels that OFC generally presents with. Symptoms are also often more severe. Generally, the presence of a palpable neck mass is also indicative of the cancer, occurring in approximately 50% of sufferers, but virtually nonexistent in individuals with OFC with a different origin.
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During this run, on 9 September 1893, Lewis Campbell became the first Vale player to score a hat-trick, and also four goals in one game, as his team brushed aside Walsall Town Swifts 5–0. They finished the season with a respectable 2–1 defeat to champions Liverpool at Anfield. Vale racked up 30 points, 10 points away from both the chance of promotion and the risk of relegation. Meshach Dean, Bob McCrindle, Billy Beats, and Alf Wood were all ever-presents, with Jimmy Scarratt and Lewis Campbell missing just one game each.
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Juvenile polyposis syndrome is an autosomal dominant syndrome characterized by increased risk of cancer of intestinal tract and extraintestinal cancer. It often presents with bleeding and obstruction of the intestinal tract along with low serum albumin due to protein loss in the intestine. The syndrome is linked to malfunction of SMAD4 a tumor suppression gene which is seen in 50% of cases. Individuals with multiple juvenile polyps have at least 10% chance of developing malignancy and should undergo abdominal colectomy with ileorectal anastomosis, and close monitoring via endoscopy of rectum.
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She is a patron of "Big Screen" at the National Film and Sound Archive.Big Screen Patron For her performance in the 1997 film The Castle, Lee was nominated for the Australian Film Institute Award for Best Supporting Actress. Lee has appeared in a number of stage productions, including Mr Kolpert with the Sydney Theatre Company and the title role in "The Virgin Mim".Plenty of Lee way Sun Herald 6 Aug 2002 (Virgin Mim) From 2008, she has hosted "Natgeo Presents with Sophie Lee" on the National Geographic channel.
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Waalkes in 2005 Waalkes' humor consists of puns and word plays as well as the use of silly and funny language, noises and body language. Parodies, for instance in form of popular songs that he revises and presents with his guitar, are typical stylistic elements. Additionally, he often imbeds satire, political innuendos and critique of time and society into his humorous performances. His Otto-Bücher (Otto-books) are regularly published and his Otto-Langspielplatten (Otto-long-playing records) became bestsellers, whereby many records attained top spots in musical charts and shops.
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Major aphthous ulceration is less common than the minor type, but produces more severe lesions and symptoms. Major aphthous ulceration presents with larger (>1 cm diameter) ulcers that take much longer to heal (10–40 days) and may leave scarring. The minor and major subtypes of aphthous stomatitis usually produce lesions on the non-keratinized oral mucosa (i.e. the inside of the cheeks, lips, underneath the tongue and the floor of mouth), but less commonly major aphthous ulcers may occur in other parts of the mouth on keratinized mucosal surfaces.
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Radiographically, the periodontal lesion often presents with alveolar bone loss in a horizontal pattern at the interproximal surface of the permanent first molars and usually horizontal bone pattern of bone loss at the interproximal surface of the incisors as the bone is thinner than at the interproximal surface of the molars. The alveolar bone loss patterns are usually bilateral and similar on both sides and has been referred to as being a ‘mirror-image’ pattern. In advanced cases the alveolar bone loss may be depicted as a horizontal bone loss pattern radiographically.
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If a patient presents with multiple symptoms such as jaundice, heart murmur, and the characteristic facial features discussed above (deep set eyes, broad brow, etc.), they are likely to be diagnosed with Alagille syndrome. A more calculated and specific diagnosis can be done with genetic testing. Next-generation sequencing can be utilized to detect single nucleotide polymorphisms (SNPs) in the affected gene(s). Multiplex ligation- dependent probe amplification (MLPA) can detect large deletions and/or insertions and microarray comparative genomic hybridization is used to improve the accuracy of MLPA.
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It can be caused by renal diseases such as bilateral renal agenesis (BRA), atresia of the ureter or urethra causing obstruction of the urinary tract, polycystic or multicystic kidney diseases, renal hypoplasia, amniotic rupture, toxemia, or uteroplacental insufficiency from maternal hypertension. The term Potter sequence was initially intended to only refer to cases caused by BRA; however, it is now commonly used by many clinicians and researchers to refer to any case that presents with oligohydramnios or anhydramnios regardless of the source of the loss of amniotic fluid.
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Sexual medicine plays a role in a wide range of medical specialties, from a primary care provider to a sexual health physician to a sexologist. A physician's role in taking a sexual history is vital in diagnosing someone who presents with a sexual dysfunction. There is some anxiety that arises when sex comes up for discussion, especially between a healthcare provider and an individual. It's reported that only 35% of primary care physicians have taken a sexual history and, due to this, there is a gap in achieving holistic healthcare.
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Giannini S, Ceccarelli F, Benedetti MG, Faldini C, Grandi G. Surgical treatment of adult idiopathic cavus foot with plantar fasciotomy, naviculocuneiform arthrodesis, and cuboid osteotomy. A review of thirty-nine cases. J Bone Joint Surg Am 2002; 84-A: 62-9 Pes cavovarus presents with the calcaneus in varus, the first metatarsal plantarflexed, and a claw-toe deformity.Meehan PL. The cavus foot in: Morrisy, RT, (Eds), Lovell and Winter's Pediatric Orthopaedics, J.B. Lippincott, Philadelphia, 1990 Radiological analysis of pes cavus in Charcot- Marie-Tooth disease shows the forefoot is typically plantarflexed in relation to the rearfoot.
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CSWS is a diagnosis of exclusion and may be difficult to distinguish from the syndrome of inappropriate antidiuretic hormone (SIADH), which develops under similar circumstances and also presents with hyponatremia. The main clinical difference is that of total fluid status of the patient: CSWS leads to a relative or overt low blood volume whereas SIADH is consistent with a normal or high blood volume (due to water reabsorption via the V2 receptor). If blood-sodium levels increase when fluids are restricted, SIADH is more likely. Additionally, urine output is classically low in SIADH and elevated in CSWS.
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Testicular self-examination (TSE) is a procedure for checking for early testicular cancer, where a man examines his own testicles and scrotum for possible lumps or swelling, performed on a regular basis starting from puberty. It is usually undertaken after a warm bath or shower while standing at home. Testicular cancer is uncommon, affects mainly men between ages 15 and 49 and typically presents with a painless testicular lump, or change in shape or texture of the testicles. Monthly self-examination of the testicles, starting at puberty, maybe an effective way of detecting testicular cancer at an early, and potentially treatable stage.
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In the Netherlands, Saint Nicholas' Eve, 5 December, became the chief occasion for gift-giving during the winter holiday season. The evening is called Sinterklaasavond ("Sinterklaas evening") or Pakjesavond ("gifts evening", or literally "packages evening"). On the evening of 5 December, parents, family, friends or acquaintences pretend to act on behalf of "Sinterklaas", or his helpers, and fool the children into thinking that "Sinterklaas" has really given them presents. This may be done through a note that is "found", explaining where the presents are hidden, as though Zwarte Piet visited them and left a burlap sack of presents with them.
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This occurs when cancerous cells break away from the insulinoma and enter the bloodstream or lymphatic system. Thus, it is possible to later develop malignancy after the initial diagnosis of insulinoma, and even after operative removal of the insulinoma. In these cases, the most common site of metastases is the liver, as well as the lymph nodes. However, the second type of diagnoses of metastatic insulinoma involves a patient who presents with symptoms of an insulinoma, and is taken for a pre-operative CT. Upon reading the radiology report, a metastatic insulinoma can be found and diagnosed immediately.
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However, the cause of the condition in males, luteinizing hormone insensitivity, does affect females, and because LH plays a role in the female reproductive system, it can result in primary amenorrhea or oligomenorrhea (absent or reduced menstruation), infertility due to anovulation, and ovarian cysts. A related condition is follicle-stimulating hormone (FSH) insensitivity, which presents with similar symptoms to those of Leydig cell hypoplasia but with the symptoms in the respective sexes reversed (i.e., hypogonadism and sexual infantilism in females and merely problems with fertility in males). Despite their similar causes, FSH insensitivity is considerably less common in comparison to LH insensitivity.
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There are other diseases associated with glomerular IgA deposits, the most common being IgA vasculitis (formerly known as Henoch–Schönlein purpura [HSP]), which is considered by many to be a systemic form of IgA nephropathy. IgA vasculitis presents with a characteristic purpuric skin rash, arthritis, and abdominal pain, and occurs more commonly in young adults (16–35 years old). HSP is associated with a more benign prognosis than IgA nephropathy. In non-aggressive IgA nephropathy there is traditionally a slow progression to chronic kidney failure in 25–30% of cases during a period of 20 years.
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The use of condoms (either male or female condoms) is one of the most effective methods of protection. Bacterial infections include: chancroid – characterised by genital ulcers known as chancres; granuloma inguinale showing as inflammatory granulomas often described as nodules; syphilis –the primary stage classically presents with a single chancre, a firm, painless, non-itchy ulcer, but there may be multiple sores; and gonorrhea that very often presents no symptoms but can result in discharge. Viral infections include human papillomavirus infection (HPV) – this is the most common STI and has many types. Genital HPV can cause genital warts.
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Albumin is an acute negative phase respondent and not a reliable indicator of nutrition status Low albumin levels can also indicate chronic malnutrition from protein losing enteropathy. This is often caused or exacerbated by ulcerative colitis, but can also be seen in cardiac disease and systemic lupus erythematosus. Broadly, protein-losing enteropathy can be caused by increased lymphatic pressure in the gastrointestinal tract as in lymphangiectasis, mucosal erosion-induced lack of absorption as in Crohn's disease and ulcerative colitis, and other diseases of malabsorption without mucosal erosions as in Celiac disease. Eosinophilic gastritis presents with epigastric pain, peripheral blood eosinophilia, anemia, and hypoalbuminemia.
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Neuroblastoma is an aggressive cancer of immature neuroblastic cells (precursors of neurons), and is one of the most common pediatric cancers, with a median age at diagnosis of two years. Adrenal neuroblastoma typically presents with a rapidly enlarging abdominal mass. Although the tumor has often spread to distant parts of the body at the time of diagnosis, this cancer is unusual in that many cases are highly curable when the spread is limited to the liver, skin, and/or bone marrow (stage IVS). Related, but less aggressive tumors composed of more mature neural cells include ganglioneuroblastoma and ganglioneuroma.
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OAFNS is a combination of FND and oculo-auriculo-vertebral spectrum (OAVS). The diagnosis of OAVS is based on the following facial characteristics: microtia (underdeveloped external ear), preauricular tags, facial asymmetry, mandibular hypoplasia and epibulbar lipodermoids (benign tumor of the eye which consists of adipose and fibrous tissue). There still remains discussion about the classification and the minimal amount of characteristics. When someone presents with FND and the characteristics of OAVS, the diagnosis OAFNS may be made. As the incidence of OAFNS is unknown, there are probably a lot of children with mild phenotypes that aren’t being diagnosed as being OAFNS.
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He then loads all the refugees onto it, promising to take care of them. By this time Shimei has reached the capital and Shogun Kiero Hakuhou, who he then presents with the Kenkaranpu. Much of the storyline revolves around the revelations of an ancient prophecy concerning the Stars, which relate to the seven stars in the Big Dipper constellation, being given human form at a time of crisis for humanity. Although all seven of the Stars are superhuman fighters, two of them are known as the Noble Spirits, and according to destiny will fight each other to take control of the Empire.
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Lesions/ulcers for herpetic gingivostomatitis may also be found on the palate and keratinzied gingivae hence aphthous ulcers can be ruled out. # Stevens–Johnson syndrome: Stevens–Johnson syndrome is characterized by early symptoms of malaise and fever, and shortly after that erythema, purpura and plaques on the skin, which often progresses to epidermal necrosis and sloughing in extreme cases. # Infectious mononucleosis - Infectious Mononucleosis presents with a high fever and lymphadenopathy, which is may or may not be presented in the symptoms of herpetic gingivostomatitis. However, upon closer oral examination, ulceration, petechiae and occasional gingivostomatitis may be spotted.
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Several patients with Hepatitis C virus (HCV) associated with mixed cryoglobulinemia (MC) have elevated levels of anti-sulfatide antibodies in their blood plasma. Mixed cryoglobulinemia (MC) is an immune disease, which typically presents with immune complex mediated vasculitis of the small vessels. It is believed there is a relationship between HCV and MC; however, the exact role of HCV in relation to the cause of MC has not yet been fully understood or discovered. Nevertheless, sphingolipid synthesis in the host, has been demonstrated to be necessary for HCV replication, which indicates that sulfatide may be involved in the replication of HCV.
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Leukocoria in a child with retinoblastoma Crossed eyes in a child with retinoblastoma The most common and obvious sign of retinoblastoma is an abnormal appearance of the retina as viewed through the pupil, the medical term for which is leukocoria, also known as amaurotic cat's eye reflex. Other signs and symptoms include deterioration of vision, a red and irritated eye with glaucoma, and faltering growth or delayed development. Some children with retinoblastoma can develop a squint, commonly referred to as "cross-eyed" or "wall-eyed" (strabismus). Retinoblastoma presents with advanced disease in developing countries and eye enlargement is a common finding.
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The Port Harcourt Carnival bears a certain uniqueness as it combines two carnivals - a purely cultural carnival and a contemporary Caribbean style carnival- in one. This gives it an edge over all other regional and continental carnivals, and presents with the principal advantage which must be consummately exploited. The Government of Rivers State recognizes Carniriv as its biggest tourism export. With economic interests increasingly identifying tourism as a viable alternative to the fossil fuel economy–especially in these parts–the state government has exhibited its commitment to developing this carnival into a regionally unrivalled and globally reckoned tourist attraction.
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Splenomegaly The typical patient with lymphocyte-variant hypereosinophilia presents with an extended history of hypereosinophilia and cutaneous allergy-like symptoms. Skin symptoms, which occur in >75% of patients, include erythroderma, pruritus, eczema, Poikiloderma, urticarial, and episodic angioedema. The symptom of episodic angioedema (i.e. soft tissue swelling of the face, tongue, larynx, abdomen, arms, or legs) in lymphocyte-variant hypereosinophilia resembles that occurring in Gleich's syndrome, a rare disease that is accompanied by secondary hypereosinophilia plus a sub-population of CD3(-), CD4(+) T cells; this involvement of the latter cell types supports the notion that Gleich's syndrome is a subtype of lymphocyte-variant hypereosiophilia.
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Careful analysis of screening results for CAH may also identify cases of congenital adrenal hypoplasia, which presents with extremely low levels of 17α-OHP. CH was added to many newborn screening programs in the 1970s, often as the second condition included after PKU. The most common cause of CH is dysgenesis of the thyroid gland After many years of newborn screening, the incidence of CH worldwide had been estimated at 1:3600 births, with no obvious increases in specific ethnic groups. Recent data from certain regions have shown an increase, with New York reporting an incidence of 1:1700.
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Sukhodolsky, et al (2017), p. 245. ADHD may also contribute to higher rates of anxiety, and aggression and anger control problems are more likely when both OCD and ADHD co-occur with Tourette's. Compulsions that resemble tics are present in some individuals with OCD; "tic-related OCD" is hypothesized to be a subgroup of OCD, distinguished from non-tic related OCD by the type and nature of obsessions and compulsions. Compared to the more typical compulsions of OCD without tics that relate to contamination, tic- related OCD presents with more "counting, aggressive thoughts, symmetry and touching" compulsions.
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Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare type of myeloid cancer in which malignant pDCs infiltrate the skin, bone marrow, central nervous system, and other tissues. Typically, the disease presents with skin lesions (e.g. nodules, tumors, papules, bruise-like patches, and/or ulcers) that most often occur on the head, face, and upper torso. This presentation may be accompanied by cPC infiltrations into other tissues to result in swollen lymph nodes, enlarged liver, enlarged spleen, symptoms of central nervous system dysfunction, and similar abnormalities in breasts, eyes, kidneys, lungs, gastrointestinal tract, bone, sinuses, ears, and/or testes.
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There are several different forms of glycine encephalopathy, which can be distinguished by the age of onset, as well as the types and severity of symptoms. All forms of glycine encephalopathy present with only neurological symptoms, including intellectual disability (IQ scores below 20 are common), hypotonia, apneic seizures, and brain malformations. With the classical, or neonatal presentation of glycine encephalopathy, the infant is born after an unremarkable pregnancy, but presents with lethargy, hypotonia, apneic seizures and myoclonic jerks, which can progress to apnea requiring artificial ventilation, and often death. Apneic patients can regain spontaneous respiration in their second to third week of life.
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Many psychiatric disorders have a genetic component and the biological family history is thus relevant. Clinical experience also suggests that a response to treatment may have a genetic component as well. Thus a patient who presents with clinical depression whose mother also suffered from the same disorder and responded well to fluoxetine would indicate that this drug would be more likely to help in the patient's disorder. Apart from the genetic factors, research has shown that illnesses in the parents such as depression and alcohol abuse are associated with a higher rate of some conditions in the children growing up in that environment.
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Ex parte Bigelow, 113 U.S. 328 (1885), was an application for a writ of habeas corpus to release the petitioner from imprisonment in the District of Columbia jail where he was held, as he alleges, unlawfully by John S. Crocker, the warden of the jail. He presents with the petition the record of his conviction and sentence in the Supreme Court of the District to imprisonment for five years under an indictment for embezzlement, and this record and the petition of the applicant present all that could be brought before the court on a return to the writ, if one were awarded..
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A redeemed Jesper delivers the presents with Klaus, and the marriage of the Krum and Ellingboe children forces the family elders to grudgingly end their feud. Jesper marries Alva and raises two children, and for the next eleven years he and Klaus deliver presents on Christmas in Smeerensburg and beyond. On the twelfth year, Klaus follows wisps of wind – which had guided him when he first met Jesper – and disappears, seemingly joining his departed wife. Jesper explains his Christmas tradition: waiting by the fireplace to see Klaus, whose spirit delivers toys to children around the world as the legend of "Santa Claus".
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Cutaneous anthrax infection in humans shows up as a boil-like skin lesion that eventually forms an ulcer with a black center (eschar), often beginning as an irritating and itchy skin lesion or blister that is dark and usually concentrated as a black dot. Cutaneous infections generally form within the site of spore penetration between two and five days after exposure. Without treatment about 20% of cutaneous skin infection cases progress to toxemia and death. Respiratory infection in humans initially presents with cold or flu- like symptoms for several days, followed by severe (and often fatal) respiratory collapse.
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Chronic lymphocytic leukemia presents with an elevated lymphocyte count and abnormal lymphocyte morphology, in which the lymphocytes have extremely dense, clumped nuclei and some cells appear smudged on the blood smear. Low lymphocyte counts (lymphopenia) may be seen in infections such as HIV/AIDS, influenza and viral hepatitis, as well as in protein-energy malnutrition, acute illnesses and drug reactions. In response to viral infections (especially infectious mononucleosis), lymphocytes may increase greatly in size, developing unusually shaped nuclei and large amounts of dark blue cytoplasm. Such cells are referred to as reactive or atypical lymphocytesBain, B et al. (2012). pp. 95–7.
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When a patient initially presents with discoid lupus, the doctor should ensure that the patient does not have systemic lupus erythematosus. The doctor will order tests to check for anti-nuclear antibodies in the patient's serum, low white blood cell levels, and protein and/or blood in the urine. In order to help with diagnosis, the doctor may peel off the top layer of scale from a patient's lesions in order to look at its underside. If the patients does indeed have discoid lupus, the doctor may see tiny spines of keratin that look like carpet tacks and are called langue au chat.
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Exposure to high level of nitrogen dioxide may lead to inflammation of the mucous membrane and the lower and upper respiratory tracts. The symptoms of acute nitrogen dioxide poisoning is non- specific and have a semblance with ammonia gas poisoning, chlorine gas poisoning, and carbon monoxide poisoning. The symptoms also resembles that of pneumonia or viral infection and other inhalational injuries but common symptoms includes rhinitis wheezing or coughing, conjunctivitis, headache, throat irritation and dyspnea which may progress to nasal fissures, ulcerations, or perforation. The patient is usually ill-appearing and presents with hypoxemia coupled with shallow rapid breathing.
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The institute specializes in language comprehension, language production, language acquisition, language and genetics, and the relation between language and cognition. Its mission is to undertake basic research into the psychological, social and biological foundations of language. The goal is to understand how human minds and brains process language, how language interacts with other aspects of mind, and how to learn languages of quite different types. The MPI for Psycholinguistics is a globally recognized center of linguistics and presents with its international archive of endangered languages a significant contribution to the preservation of the common heritage of mankind.
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Minimal change disease is characterised as a cause of nephrotic syndrome without visible changes in the glomerulus on microscopy. Minimal change disease typically presents with edema, an increase in proteins passed from urine and decrease in blood protein levels, and an increase in circulating lipids (i.e., nephrotic syndrome) and is the most common cause of the nephrotic syndrome in children. Although no changes may be visible by light microscopy, changes on electron microscopy within the glomeruli may show a fusion of the foot processes of the podocytes (cells lining the basement membrane of the capillaries of glomerulus).
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The disorder commonly presents with renal disease that in general is advanced or at an end stage. Associated signs and symptoms of their renal disease may include fatigue, dehydration, blood in urine, and/or other evidence for the presence of the nephrotic syndrome or renal failure. Further studies may find that these individuals have histological or other evidence of LECT2 amyloid deposition in the liver, lung, spleen, kidney, and/or adrenal glands but nonetheless they rarely show any symptoms or signs attributable to dysfunction in these organs. Unlike many other forms of systemic amyloidosis, LECT2 deposition has not been reported to be deposited in the myocardium or brain of affected individuals.
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On all films since Broccoli's death, the opening credit is "Albert R. Broccoli's Eon Productions presents", with "Ltd." usually added after "Productions" in the film proper.DVD and Blu-ray copies of Eon's Bond films. The 1965 film Thunderball differs from the others in how it credits Saltzman and Broccoli; due to a legal agreement with Kevin McClory related to the rights to Ian Fleming's original novel, McClory received producer credit on the film, with Saltzman and Broccoli credited as executive producers. This agreement also gave McClory the rights to remake Thunderball in the future, resulting in the 1983 non-EON production, Never Say Never Again.
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Clinical signs and symptoms of complement-mediated TMA can include abdominal pain, confusion, fatigue, edema (swelling), nausea/vomiting and diarrhea. aHUS often presents with malaise and fatigue, as well as microangiopathic anemia. However, severe abdominal pain and bloody diarrhea are unusual. Laboratory tests may also reveal low levels of platelets (cells in the blood that aid in clotting), elevated lactate dehydrogenase (LDH, a chemical released from damaged cells, and which is therefore a marker of cellular damage), decreased haptoglobin (indicative of the breakdown of red blood cells), anemia (low red blood cell count)/schistocytes (damaged red blood cells), elevated creatinine (indicative of kidney dysfunction), and proteinuria (indicative of kidney injury).
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Twin studies indicate that the disorder is often inherited from the person's parents, with genetics determining about 75% of cases in children and 35% to potentially 75% of cases in adults. Siblings of children with ADHD are three to four times more likely to develop the disorder than siblings of children without the disorder. Arousal is related to dopaminergic functioning, and ADHD presents with low dopaminergic functioning. Typically, a number of genes are involved, many of which directly affect dopamine neurotransmission. Those involved with dopamine include DAT, DRD4, DRD5, TAAR1, MAOA, COMT, and DBH. Other genes associated with ADHD include SERT, HTR1B, SNAP25, GRIN2A, ADRA2A, TPH2, and BDNF.
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LECT2 amyloidosis presents with renal disease that in general is slowly progressive and at the time of presentation is of varying severity ranging from early findings of proteinuria or small elevations in blood urea nitrogen and/or creatinine to findings of end stage renal disease. At presentation, many individuals are elderly and suffer serious kidney dysfunction. They may have histological evidence of LECT2 amyloid deposition in the liver, lung, spleen, kidney, and adrenal glands of rarely show any symptoms or signs attributable to dysfunction in these organs. Unlike many other forms of systemic amyloidosis, LECT2 deposition has not been reported to be deposited in the myocardium or brain of afflicted individuals.
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Both excess and inadequate potassium can be life-threatening. A common presentation of hyperkalemia is in the patient with end-stage renal disease who has missed a dialysis appointment and presents with weakness, nausea, and broad QRS complexes on the electrocardiogram. (Note however that patients with chronic kidney disease are often more tolerant of high potassium levels as their body often adapts to it.) Several medications, for example the antibiotic trimethoprim/sulfamethoxazole or an ACE inhibitor, can also lead to the development of significant hyperkalemia. The electrocardiogram will show tall, peaked T waves (often larger than the R wave) or can degenerate into a sine wave as the QRS complex widens.
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Laboratory tests are generally conducted when the patient presents with signs and symptoms that may be characteristic of kidney impairment. They are not primarily used to diagnose kidney cancer, due to its asymptomatic nature and are generally found incidentally during tests for other illnesses such as gallbladder disease. In other words, these cancers are not detected usually because they do not cause pain or discomfort when they are discovered. Laboratory analysis can provide an assessment on the overall health of the patient and can provide information in determining the staging and degree of metastasis to other parts of the body (if a renal lesion has been identified) before treatment is given.
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Volvulus of the large colon usually occurs where the mesentery attaches to the body wall, but may also occur at the diaphragmatic or sternal flexures, with rotations up to 720 degrees reported. It is most commonly seen in postpartum mares, usually presents with severe signs of colic that are refractory to analgesic administration, and horses often lie in dorsal recumbency. Abdominal distention is common due to strangulation and rapid engorgement of the intestine with gas, which then can lead to dyspnea as the growing bowel pushes against the diaphragm and prevents normal ventilation. Additionally, compression can place pressure on the caudal vena cava, leading to pooling of blood and hypovolemia.
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It is only when bradycardia presents with signs and symptoms of shock that it requires emergency treatment with transcutaneous pacing. False capture with visible phantom beats Some common causes of hemodynamically significant bradycardia include myocardial infarction, sinus node dysfunction and complete heart block. Transcutaneous pacing is no longer indicated for the treatment of asystole (cardiac arrest associated with a "flat line" on the ECG), with the possible exception of witnessed asystole (as in the case of bifascicular block that progresses to complete heart block without an escape rhythm). During transcutaneous pacing, pads are placed on the patient's chest, either in the anterior/lateral position or the anterior/posterior position.
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Airport malaria, sometimes known as baggage, luggage or suitcase malaria, occurs when a malaria infected female Anopheles mosquito travels by aircraft from a country where malaria is common, arrives in a country where malaria is usually not found, and bites a person at or around the vicinity of the airport, or if the climate is suitable, travels in luggage and bites a person further away. The infected person usually presents with a fever in the absence of a recent travel history. There is often no suspicion of malaria, resulting in a delay in diagnosis and often death. Other causes of imported malaria need to be excluded first.
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When C. trachomatis presents in the eye in the form of trachoma it begins by gradually thickening the eyelids, and eventually begins to pull the eyelashes into the eyelid. In the form of inclusion conjunctivitis the infection presents with redness, swelling, mucopurulent discharge from the eye, and most other symptoms associated with adult conjunctivitis. When C. trachomatis is in the lungs in the form of a respiratory infection it typically has symptoms of a runny or stuffy nose, low-grade fever, hoarseness of voice, as well as other symptoms associated with general pneumonia. C. trachomatis may latently infect the chorionic villi tissues of pregnant women, thereby impacting pregnancy outcome.
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Despite the functional aspects of ICAM-4, its apparent absence in LW(a-b-) and Rhnull phenotypes does not appear to lead to any obvious pathological effects. ICAM-4 expression is elevated on sickle red cells and its binding to αv integrins on the endothelial cells may cause the pain associated with sickle cell crises. Auto anti-LW is not uncommon as an autoantibody but usually presents with transient suppression of the LW antigen in genetically LW+ individuals, and so appears to be an alloantibody. True alloanti-LW is a very rare occurrence, with only two known examples of alloanti-LWab, produced by patients with an LW(a-b-) phenotype.
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In this context, PAX3-FOXO1 both (1) drives the expression of MYC, MYCN and even MYOD1 (a transcription factor highly expressed in all RMS subtypes) but also (2) co- binds with these master transcription factors at super enhancers to support cancer growth. Furthermore, it was demonstrated that FP-RMS subtypes were especially sensitive to inhibitors (such as JQ1) of a super enhancer bound protein BRD4. Embryonal RMS usually presents with a loss of heterozygosity (LOH) in the short arm of chromosome 11 (p11,15.5). This region is associated with multiple oncogenes, and the potential loss-of-function of this region is likely associated with the loss of a tumor suppressor.
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Batsford co-created the creative network Project X Presents with Marc Reck, Anne-Marie Pope and Anthony Ramm, producing a series of five events dubbed "Omnimedia Experiences" beginning with Like Fxck in July 2006 in the Epic Skate Park in Birmingham. The events featured artists from a wide range of disciplines coming together to blend their work into a seamless, immersive event lasting up to seven hours, usually presented across three stages, with the audience in the middle The Birmingham Post described the event as "destabilising the established role of the ‘spectator’ in performance theatre and drawing you in to an impressively eclectic and complex mix of art forms".
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The disease typically presents with joint pain, high fevers, a salmon-pink macular or maculopapular rash, enlargement of the liver and spleen, swollen lymph nodes, and a neutrophil-predominant increased white blood cell count in the blood. Tests for rheumatoid factor and anti-nuclear antibodies are usually negative and serum ferritin is markedly elevated. Patients experiencing a flare-up from Adult-onset Still's disease usually report extreme fatigue, swelling of the lymph nodes and, less commonly, fluid accumulation in the lungs and heart. In rare cases, AOSD can cause life-threatening complications, including hemophagocytic lymphohistiocytosis, IVDC, fulminant hepatitis, or disabling conditions such as aseptic meningitis and sensorineural hearing loss.
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The symptoms of pulmonary hypertension include the following: Less common signs/symptoms include non-productive cough and exercise-induced nausea and vomiting. Coughing up of blood may occur in some patients, particularly those with specific subtypes of pulmonary hypertension such as heritable pulmonary arterial hypertension, Eisenmenger syndrome and chronic thromboembolic pulmonary hypertension. Pulmonary venous hypertension typically presents with shortness of breath while lying flat or sleeping (orthopnea or paroxysmal nocturnal dyspnea), while pulmonary arterial hypertension (PAH) typically does not. Other typical signs of pulmonary hypertension include an accentuated pulmonary component of the second heart sound, a right ventricular third heart sound, and parasternal heave indicating a hypertrophied right ventricle.
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The album was certified double gold in the UK; the band was nominated for a Best Breakthrough Award at The South Bank Show Awards and for Best Dancefloor Filler at the NME Awards. They were also second on the bill on the Shockwaves NME Awards Tour in January and February 2009, playing alongside headliner Glasvegas and other up-and-coming bands White Lies and Florence and the Machine. In March 2009, Friendly Fires co-headlined with White Lies on an American equivalent of the tour called NME Presents, with The Soft Pack supporting. On 21 July 2009, Friendly Fires was nominated for the Mercury Music Prize.
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Immunohistochemical detection of C. burnetii in resected cardiac valve of a 60-year-old man with Q fever endocarditis, Cayenne, French Guiana, monoclonal antibody against C. burnetii and hematoxylin were used for staining: Original magnification ×50 The ID50 (the dose needed to infect 50% of experimental subjects) is one via inhalation; i.e., inhalation of one organism will yield disease in 50% of the population. This is an extremely low infectious dose (only 1-10 organisms required), making C. burnetii one of the most infectious known organisms. Disease occurs in two stages: an acute stage that presents with headaches, chills, and respiratory symptoms, and an insidious chronic stage.
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IgA nephropathy, also known as Berger's disease, is the most common type of glomerulonephritis, and generally presents with isolated visible or occult hematuria, occasionally combined with low grade proteinuria, and rarely causes a nephritic syndrome characterised by protein in the urine, and visible blood in the urine. IgA nephropathy is classically described as a self-resolving form in young adults several days after a respiratory infection. It is characterised by deposits of IgA in the space between glomerular capillaries. Henoch–Schönlein purpura refers to a form of IgA nephropathy, typically affecting children, characterised by a rash of small bruises affecting the buttocks and lower legs, with abdominal pain.
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Severity of the hearing impairment is greatly variable, as it ranges from a mild hearing defect that occurs in mid or advanced age to a progressive hearing loss that is evident in the first years of life and rapidly evolves to severe deafness. Kidney damage occurs in about 25% of patients. It presents with proteinuria and often progresses to kidney failure, which, in its most severe forms, may require dialysis and/or kidney transplantation. Around 20% of patients develop presenile cataracts. About 50% of MYH9-RD patients present chronic or intermittent elevation of liver transaminases or gamma-glutamyl transferases: this alteration appears to be benign, as no patients showed evolution to liver dysfunction.
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To diagnose gynecomastia, a thorough history and physical examination are obtained by a physician. Important aspects of the physical examination include evaluation of the male breast tissue with palpation to evaluate for breast cancer and pseudogynecomastia (male breast tissue enlargement solely due to excess fatty tissue), evaluation of penile size and development, evaluation of testicular development and an assessment for masses that raise suspicion for testicular cancer, and proper development of secondary sex characteristics such as the amount and distribution of pubic and underarm hair. Gynecomastia usually presents with bilateral involvement of the breast tissue but may occur unilaterally as well. A review of the medications or illegal substances an individual takes may reveal the cause of gynecomastia.
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Follicular lymphoma generally presents with an indolent course, some patients do not need treatments for several years, while others whose cancer has widely spread to lymph nodes or organs need treatment immediately. In some cases, the disease can transform into an aggressive type of lymphoma, mostly diffuse large B-cell lymphoma (DLBCL). Patients who have stage I or II FL may be closely monitored without receiving treatment, they may be treated with radiation therapy alone or with chemotherapy. Patients who are in stage II but have bulky disease, in stage III/IV or have relapsed or refractory disease may be treated with therapies depending on the patient's age, overall health, disease progression, symptoms, and the patient's choice.
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Because the relative frequency of certain queries is highly correlated with the percentage of physician visits in which a patient presents with influenza- like symptoms, an estimate of weekly influenza activity can be reported. A more sophisticated model for inferring influenza rates from Google Trends, capable of overcoming the mistakes of its predecessors has been proposed by Lampos et al. The use of google trends to study a wide range of medical topics is becoming more widespread. Studies have been performed examining such diverse topics as use of tobacco substitutes,Cavazos-Rehg, Patricia A., Melissa J. Krauss, Edward L. Spitznagel, Ashley Lowery, Richard A. Grucza, Frank J. Chaloupka, and Laura Jean Bierut.
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In some senses, the process of diagnosis is always a matter of assessing the likelihood that a given condition is present in the patient. In a patient who presents with haemoptysis (coughing up blood), the haemoptysis is very much more likely to be caused by respiratory disease than by the patient having broken their toe. Each question in the history taking allows the medical practitioner to narrow down their view of the cause of the symptom, testing and building up their hypotheses as they go along. Examination, which is essentially looking for clinical signs, allows the medical practitioner to see if there is evidence in the patient's body to support their hypotheses about the disease that might be present.
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The first iteration of Davis's company started in 2001 as a production studio at Image Comics, where its founder Darren G. Davis developed the company's signature series 10th Muse and The Legend of Isis. This iteration came to an end with the company declared bankrupt in 2003. Davis's revived company, then known as Bluewater Productions, became a publisher in May 2007 with the signature series Ray Harryhausen Presents, which was produced in conjunction with filmmaker Ray Harryhausen until 2009. Other signature series, including Vincent Price Presents, produced in conjunction with the daughter of the actor Vincent Price,Immortal After All... Vincent Price Comes to Comic Books, Newsarama, June 13, 2008 and William Shatner Presents, with actor William Shatner, followed.
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Lyrically, the song tells the story of a couple who are preparing to exchange Christmas presents with each other as part of the Secret Santa Christmas tradition, but have decided to complete the swap intimately and at midnight. When interviewed during a Billboard podcast in 2018, Stefani herself described the song as better suited for adults. She said: "['Secret Santa'] sort of reminds me of like a 'Santa Baby' lane ... in the sense of like a little sexy song." Within the chorus, Stefani sings: "Let's play Secret Santa in the dark / Don't tell anybody where we are / There's no limit to the ways that we can celebrate / A midnight gift exchange of heart".
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During 1975 and 1976, Rocio virus was responsible for several epidemics of meningoencephalitis in coastal communities in southern São Paulo, Brazil. The outbreaks affected over 1,000 people and killed about 10% of those infected, but apparently responded well to treatment for viral encephalitides. The disease progresses rapidly after onset, with patients dying within 5 days of symptoms first appearing. The disease first presents with fever, headache, vomiting, and conjunctivitis, then progresses to neurological symptoms (confusion, disorientation, etc.) and muscle weakness; about one-third of cases enter a coma, and a third of those patients die, although supportive care such as intensive nursing and symptomatic treatment might reduce the case fatality rate to 4%.
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Psoriasis can also cause changes to the nails, such as pitting or separation from the nail bed, onycholysis, hyperkeratosis under the nails, and horizontal ridging. Psoriasis classically presents with scaly skin lesions, which are most commonly seen over extensor surfaces such as the scalp, natal cleft and umbilicus. In psoriatic arthritis, pain can occur in the area of the sacrum (the lower back, above the tailbone), as a result of sacroiliitis or spondylitis, which is present in 40% of cases. Pain can occur in and around the feet and ankles, especially enthesitis in the Achilles tendon (inflammation of the Achilles tendon where it inserts into the bone) or plantar fasciitis in the sole of the foot.
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The Neolithic presents with 37 sites found during excavations of the settlement "Dvuhozernoe-I", the ritual complex "Ostrov-II", and the grave field "Old-Lybaevo-IV". 6 of these belong to the Koshkino archaeological culture, 12 to the Sosnovka-Ostrov culture, 11 to the Boborykino, 3 to the Poludenskoe and 5 don't have a reliable cultural attribution. According to Eugene Volkov, the earliest Neolithic culture of the Ingala Valley should be considered the Koshkino (middle 6th millennium BC - late 5th millennium BC), and the Sosnovka-Ostrov (middle 5th millennium BC - 4th millennium BC) was the next. Boborykino culture (late 5th millennium BC - late 4th millennium BC) coexisted with the Koshkinskino and Sosnovka-Ostrov.
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Choosing to appear as familiar as possible to his mainland hosts, Soong spoke his greetings in the local dialect in each of the cities that he visited. Beyond sentimental visits, the important political aspect of his tour comes from his visit to Beijing. There, he shook hands with Hu Jintao, General Secretary of the Communist Party of China, and exchanged presents with him; Soong gave Hu a work of glass art from Liuli Gongfang, and received a piece of Jingdezhen porcelain from Hu. Soong was only the second major political figure from Taiwan to ever do so. The carefully scripted red-carpet ceremony was identical to the previous greeting for KMT Chairman Lien Chan.
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Foreman takes a job at Mercy Hospital in New York, and he immediately goes out of his way to conduct differential diagnoses with a calm head and professional attitude, almost the exact opposite of House. However, when a patient presents with a condition with similar symptoms to the patient he killed, Foreman goes against regulations (like House) to save the patient's life, which he does. Despite making a life-saving call, Foreman's administrator fires him due to violating regulations. Foreman is then re-hired by Dr. Lisa Cuddy to serve as a partner of sorts with Dr. House and to act as the "eyes and ears" of Dr. Cuddy on House's team.
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Predominantly diffuse follicular lymphoma with 1p36 deletion is a rare subtype of FL in which involved lymph nodes show infiltrations of centrocytes and centoblasts that generally do not form the nodular, swirling patterns characteristic of most types of FL. In addition, these cells lack the t(14:18)(q32:q21.3) translocation commonly found in other FL types but, similar to many FL cases, have a deletion in the terminal part of the short (i.e. "p") arm of chromosome 1 that encodes the TNFRSF14 gene (see pathophysiology section). Predominantly diffuse follicular lymphoma with 1p36 deletion usually presents with bulky enlargements of inguinal (i.e. groin) lymph nodes but may present with enlargements of the axillary (i.e.
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Peutz–Jeghers syndrome is an autosomal dominant syndrome that presents with hamartomatous polyps, which are disorganized growth of tissues of the intestinal tract, and hyperpigmentation of the interlining of the mouth, lips and fingers. The syndrome was first noted in 1896 by Hutchinson, and later separately described by Peutz, and then again in 1940 by Jeghers. The syndrome is associated with malfunction of serine- threonine kinase 11 or STK 11 gene, and has a 2% to 10% increase in risk of developing cancer of the intestinal tract. The syndrome also causes increased risk of extraintestinal cancer such as that involving breast, ovary, cervix, fallopian tubes, thyroid, lung, gallbladder, bile ducts, pancreas, and testicles.
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Characteristic injuries associated with AHT include retinal bleeds, multiple fractures of the long bones, and subdural hematomas (bleeding in the brain). These signs have evolved through the years as the accepted and recognized signs of child abuse. Medical professionals strongly suspect shaking as the cause of injuries when a young child presents with retinal bleed, fractures, soft tissue injuries or subdural hematoma, that cannot be explained by accidental trauma or other medical conditions.B.G.Brogdon, Tor Shwayder, Jamie Elifritz Child Abuse and its Mimics in Skin and Bone Retinal bleeds occur in around 85% of AHT cases; the type of retinal bleeds are particularly characteristic of this condition, making the finding useful in establishing the diagnosis.
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In 1856 Reuter left Treptow and established himself at Neubrandenburg, resolving to devote his whole time to literary work. His next book (published in 1858) was Kein Hüsung, a verse epic in which he presents with great force and vividness some of the least attractive aspects of village life in Mecklenburg. This was followed, in 1860, by Hanne Nüte un de lütte Pudel, the last of the works written by Reuter in verse. In 1861 Reuter's popularity was largely increased by Schurr-Murr, a collection of tales, some of which are in standard German, but this work is of slight importance in comparison with the series of stories, entitled Olle Kamellen ("old stories of bygone days").
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The presence of presenile cataract, noticeable in galactosemic infants as young as a few days old, is highly associated with two distinct types of galactosemia: GALT deficiency and to a greater extent, GALK deficiency. An impairment or deficiency in the enzyme, galactose-1-phosphate uridyltransferase (GALT), results in classic galactosemia, or Type I galactosemia. Classic galactosemia is a rare (1 in 47,000 live births), autosomal recessive disease that presents with symptoms soon after birth when a baby begins lactose ingestion. Symptoms include life-threatening illnesses such as jaundice, hepatosplenomegaly (enlarged spleen and liver), hypoglycemia, renal tubular dysfunction, muscle hypotonia (decreased tone and muscle strength), sepsis (presence of harmful bacteria and their toxins in tissues), and cataract among others.
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Although there are a multitude of varying appearances, the id reaction often presents with symmetrical red patches of eczema with papules and vesicles, particularly on the outer sides of the arms, face and trunk which occur suddenly and are intensely itchy occur a few days to a week after the initial allergic or irritant dermatitis. Most commonly, athlete's foot can lead to localised vesicles on hands, bacterial infections to erythema nodosum and herpes simplex virus to erythema multiforme. The diagnosis is frequently made by treating the initial triggering skin problem and observing the improvement in the eczematous rash. Both the initial skin problem and the id reaction must be observed to make the diagnosis.
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Apart from that he is the writer of TV series for children like Kulderzipken and Dag Sinterklaas and he is also author of the theater piece Frankenstein by Smrntwsk Alleen (1989). On top on that, he wrote some music texts for De Nieuwe Snaar. The Dag Sinterklaas series he wrote about Sinterklaas (=Saint Nicholas, European origin of Santa Claus) since the early 1990s gave children in Flanders, Belgium a view on the daily life of the holy man. Also, it explained some of the questions children have around the event: why Zwarte Piet (Black Peter) is black (not his original skin colour, but because of sliding through the chimney) and how Sinterklaas acquires the presents (with a special kind of money).
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In 1968 Davies, Dent and Watson produced a historic case study where they reviewed 200 cases of previously diagnosed primary hyperparathyroidism and found the majority of these cases should be reclassified as tertiary. These were important findings as it allowed an understanding into distinguishing features of primary, secondary and tertiary hyperparathyroidism which then allows appropriate medical treatment. It is now understood that tertiary hyperparathyroidism is defined as the presence of hypercalcemia, hyperphosphatemia and parathyroid hormone due to terminally biased parathyroid-bone-kidney feedback loop. Although there is still conjecture as to whether tertiary hyperparathyroidism is also due to adenomatous growth or hyperplasia it is clear that tertiary hyperparathyroidism presents with some form of tissue enlargement in all four parathyroid glands.
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Blind since birth (as was his elder brother), he attended New College Worcester, which was then known as the Worcester College for the Blind. He was a regular presenter on BBC Radio Solent from the station's launch in 1971 until November 2006, when he was one of several long-serving and well-respected presenters who were sacked in an attempt to improve listener figures. He currently presents (with others) You and Yours and (since 1974) In Touch (both BBC Radio 4), a programme for blind and partially sighted people, and regularly contributes to other science, news or educational programmes to talk about disabilities. He was the presenter of Channel 4's Same Difference (1987–1989) and Central Television's Link (1989–1991).
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Since IgA nephropathy commonly presents without symptoms through abnormal findings on urinalysis, there is considerable possibility for variation in any population studied depending upon the screening policy. Similarly, the local policy for performing kidney biopsy assumes a critical role; if it is a policy to simply observe patients with isolated bloody urine, a group with a generally favourable prognosis will be excluded. If, in contrast, all such patients are biopsied, then the group with isolated microscopic hematuria and isolated mesangial IgA will be included and ‘improve’ the prognosis of that particular series. Nevertheless, IgA nephropathy, which was initially thought to be a benign disease, has been shown to not be a benign disease, particularly if the patient presents with an aggressive form.
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In 2018, the then Paraguayan Foreign Minister Eladio Loizaga said at a press conference that he called in Hedges to express discomfort over a tweet that Hedges had made after the Supreme Court of Paraguay overturned the conviction of 12 farmers in a case relating to the violent deaths of 6 police officers and 11 rural workers in 2012. Hedges had tweeted: "How beautiful is the smile of freedom," above a photograph of one of the freed men who is seen smiling and embracing a woman. Hedges told reporters that he was merely reacting to a 'human moment' shown by the photograph. In 2019, Hedges was received by the senior commanding officers of the Paraguayan Navy and exchanged presents with them.
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Pal co-wrote the 2007 Indian comedy, Loins Of Punjab Presents, with Manish Acharya which The New York Times called 'a witty musical comedy'. In 2009, his play, The President Is Coming, was made into a Bollywood film The President Is Coming made by producer Rohan Sippy. As a stand up comedian, Pal started out with The British Comedy Store when they opened in Mumbai in 2010 and has since toured across the nation with his acclaimed one man show, The Nation Wants To Know in Mumbai, New Delhi, Kolkata, Shillong, Bangalore, and Pune. His first play Chaos Theory, a love story between two Indian professors, was written in New York City, and performed in various productions around the United States.
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Clinical diagnostic features are lifelong eruptions of pityriasis versicolor-like macules, flat wart-like papules, one to many cutaneous horn-like lesions, and development of cutaneous carcinomas. Patients present with flat, slightly scaly, red-brown macules on the face, neck, and body, recurring especially around the penial area, or verruca-like papillomatous lesions, seborrheic keratosis-like lesions, and pinkish-red plane papules on the hands, upper and lower extremities, and face. The initial form of EV presents with only flat, wart-like lesions over the body, whereas the malignant form shows a higher rate of polymorphic skin lesions and development of multiple cutaneous tumors. Generally, cutaneous lesions are spread over the body, but some cases have only a few lesions which are limited to one extremity.
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Fleeing from McQueen's bounty hunter character Josh Randall, Homeier's character's foot slips and he accidentally falls to his death from a cliff. He appeared in a 1955 episode of Alfred Hitchcock Presents, with co-star Joanne Woodward entitled "Momentum". Homeier appeared as Kading in an episode of the NBC western Jefferson Drum ("The Post", 1958), starring Jeff Richards. In 1959, he appeared as a drover named Lucky in Rawhide, Incident of the Blue Fire. In 1960, Skip appeared on an episode of The Rifleman: The Spoiler as Brud Evans. Then, from 1960 to 1961, he starred in the title role in Dan Raven, a short- lived NBC crime drama set on Sunset Strip of West Hollywood, California, with a number of celebrities playing themselves in guest roles.
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He announced his resignation a year later, claiming he was tiring of the constant travel between his home in Launceston and the WIN Television studio in Hobart. After a number of years focusing his public relations work and his political aspirations, Titmus returned to television in 2015 as a producer at 7 News Brisbane after his family relocated to Queensland due to a lack of swimming opportunities in Tasmania for his daughter.Titmus on move, Rob Shaw, The Examiner, 19 May 2015. Retrieved 16 October 2016 From December 2015, Titmus has also served as a relief co-presenter on Channel 7's regional bulletins, often filling in for Rob Brough on some of the local bulletins Brough usually co-presents with Joanne Desmond that air throughout Queensland.
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Infantile pyknocytosis typically presents with neonatal jaundice and severe anemia, often requiring blood transfusions. The associated hemolytic anemia is often transient with peak incidence at 3–4 weeks, with spontaneous and complete resolution by four to six months of life. An etiology for this condition has not been established but some evidence, including the presence of dehydrated red cells on peripheral blood smear that seem to have undergone oxidative stress, points to causes that include deficiency of antioxidants such as vitamin E or the presence of an oxidative factor. The diagnosis of infantile pyknocytosis is essentially based on the peripheral blood smear, with additional diagnostic investigations to rule out similarly presenting conditions such as glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase deficiency.
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On December 7, 2007, the Canada-based Toronto Sun newspaper published a report on the arrest of the alleged Internet predator Chris Forcand. Forcand, 53, was charged with two counts of luring a child under the age of 14, attempt to invite sexual touching, attempted exposure, possessing a dangerous weapon, and carrying a concealed weapon. The report stated that Forcand was already being tracked by "cyber-vigilantes who seek to out anyone who presents with a sexual interest in children" before police investigations commenced. The Global Television Network report identified the group responsible for Forcand's arrest as a "self-described Internet vigilante group called Anonymous" who contacted the police after some members were "propositioned" by Forcand with "disgusting photos of himself".
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The DRESS syndrome is a severe immunological drug reaction. It differs from other drug reactions in that it: a) is caused by a particular set of drugs; b) typically occurs after a delay of 2 to 8 weeks following intake of an offending drug; c) presents with a specific set of signs and symptoms (i.e. modest or extreme elevations in blood eosinophil and atypical lymphocyte counts; acute onset of a skin rash; lymphadenopathy; fever; neuralgia; and involvement of at least one internal organ such as the liver, lung, or heart; d) develops in individuals with particular genetic predispositions; and e) involves reactivation of latent viruses, most commonly human herpesvirus 6 or more rarely human herpes virus 5 (i.e. human cytomegalovirus), human herpesvirus 7, and human herpesvirus 4 (i.e.
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Due to organic amnesia often being difficult to detect, defining between organic and psychogenic amnesia is not easy and often context of precipitating experiences are considered (for example, if there has been drug abuse) as well as the symptomology the patient presents with. Psychogenic amnesia is supposed to differ from organic amnesia qualitatively in that retrograde loss of autobiographical memory while semantic memory remains intact is said to be specific of psychogenic amnesia. Another difference that has been cited between organic and psychogenic amnesia is the temporal gradient of retrograde loss of autobiographical memory. The temporal gradient of loss in most cases of organic amnesia is said to be steepest at its most recent premorbid period, whereas for psychogenic amnesia the temporal gradient of retrograde autobiographical memory loss is said to be quite consistently flat.
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Because of the very short time between presentation of mastitis and breast cancer in this study it is considered very unlikely that the inflammation had any substantial role in carcinogenesis, rather it would appear that some precancerous lesions may increase the risk of inflammation (hyperplasia causing duct obstruction, hypersensitivity to cytokines or hormones) or the lesions may have common predisposing factors. A very serious type of breast cancer called inflammatory breast cancer presents with similar symptoms as mastitis (both puerperal and nonpuerperal). It is the most aggressive type of breast cancer with the highest mortality rate. The inflammatory phenotype of IBC is thought to be mostly caused by invasion and blocking of dermal lymphatics, however it was recently shown that NF-κB target genes activation may significantly contribute to the inflammatory phenotype.
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Chris was one of the original line up of CBeebies presenters, alongside Pui Fan Lee, Sidney Sloane, and Sue Monroe everyday. From March 2007 until his departure on 26 January 2009 he presented alongside Lee from 9:00 am – 3:00 pm with Discover and Do, then the Bedtime Hour from 6:00 pm and again on BBC Two in the mornings. He starred in Step Inside as Mr Mopple the storyteller before going on to write and star in Show Me Show Me. Show Me Show Me, which he co-presents with Pui Fan Lee, is broadcast on CBeebies. The first 40 half-hour episodes were broadcast on the CBeebies channel, BBC One and BBC Two from Monday 6 July 2009 every weekday at 10:00 am and 1:30 pm.
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Brough is joined by Joanne Desmond as a co-presenter on the Cairns, Townsville, Central Queensland and Darling Downs editions of Seven News, while Brough continues to present the Mackay, Wide Bay and Sunshine Coast editions by himself. When Brough is away, Steve Titmus joins Joanne Desmond on the editions that she usually co-presents with Brough, while Desmond fills in for Brough by herself on the bulletins he usually presents solo. With the studio producing seven 30-minute news bulletins each weeknight, along with additional afternoon and evening updates, it's one of the busiest news studios in Australia, making Brough one of the country's busiest news presenters. Brough can now be seen reading regional editions of Seven News as far south as Stanthorpe, as far north as Port Douglas and as far west as the Central Highlands in Central Queensland.
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Even with the gene change, it may still take time before a cell actually does develop that is cancerous as a result, and the gene may in some cases still partially operate to control tumours, therefore cancer from FAP takes many years to develop and is almost always an adult-onset disease. The second form of FAP, known as attenuated familial adenomatous polyposis has the APC gene functional but slightly impaired. It is therefore somewhat able to operate as usual. Attenuated FAP still presents a high 70% lifetime risk of cancer (as estimated), but typically presents with far fewer polyps (typically 30) rather than the hundreds or thousands usually found in FAP, and arises at an age when FAP is usually no longer considered likely—typically between 40 and 70 years old (average 55) rather than the more usual 30s upward.
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Chrismukkah was named for the first time, and prominently featured, in the FOX television program The O.C. (2003–2007). Show creator Josh Schwartz used the holiday (which the writers almost named "Hanimas") to depict, he later said, On The O.C., as a way to merge his parents' two faiths, Seth Cohen claims to have "created the greatest superholiday known to mankind" when he was six years old. The series included annual Chrismukkah episodes for every season of its run. Particulars of when exactly the holiday was celebrated were not given; Seth simply said in the first season's Chrismukkah episode that it was "eight days of presents, followed by one day of many presents," with a stress on the word "many" (this was repeated in the second season's Chrismukkah episode by Seth's new brother Ryan, with an added "many").
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Primary follicular lymphoma of the testis (PFLT), also termed testicular follicular lymphoma, was classified as a distinct form of FL by the World Health Organization in 2016. It is an extremely rare disease that has been recognized as occurring primarily in children and adolescents but also has been reported in 5 adults. PFLT differs from cases of typical follicular lymphoma that involve the testis in that it more often occurs in children and adolescents; involves malignant B-cells that do have the t(14:18)q32:q21) translocation; and presents with disease that is strictly limited to the testis. While similar to pediatric-type follicular lymphoma in not involving cells that bear the t(14:18)q32:q21) translocation, PFLT differs from the former disease in that it is limited to the testis and involves malignant cells that do not express Bcl2.
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Gurning has appeared in festivals such as the Progetto Martha Argerich in Lugano, the Schleswig-Holstein Musik Festival in Denmark, the piano International Festival de La Roque-d'Anthéron in France, the Sapporo Music Festival in Japan, the International Piano Festival of Obidos (Portugal), the Saratoga Chamber Music Festival and the Tanglewood Music Festival (United States) and the Verbier Festival in China. Gurning has played with the Boston Symphony Orchestra, the Philadelphia Orchestra, the Orchestra della Svizzera Italiana, the Orchestre Philharmonique de Radio France, the Orchestre National de Belgique, the Orchestre de Chambre de Lausanne with conductors such as Myung-Whun Chung, Charles Dutoit, and Christian Zacharias. More recently, Gurning toured Europe performing Bach’s Goldberg Variations. The recording career of Gurning started with a ‘Choc’ award from Le Monde for his first solo album, in the series 'Martha Argerich Presents', with works of Stravinsky and Debussy.
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290 King led Howitt to Wills' grave site where they reburied his remains and made an inscription on a nearby tree. Burke was then buried. Once King was well enough to travel, Howitt decided to return southward but would not leave without registering his gratitude to the Aboriginal people Howitt's diary entry of 24 September 1861 notes: > Two days after we camped here the natives left and have not been seen since. > I could not think of leaving without showing them that we could appreciate > and reward the kindness they had shown to Burke's party and particularly to > King...They left, making signs expressive of friendship, carrying their > presents with them.Howitt 1857-73 On 1 March at Camp 32 (Cooper Creek) Howitt records: > Returned today, keeping much the same course, but nearer the creek over a > succession of very rotten flats, timbered with box.
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The 2002 martial arts epic Hero presented the same narrative several different times, as recounted by different storytellers, but with both factual and aesthetic differences. Similarly, in the whimsical 1988 Terry Gilliam film The Adventures of Baron Munchausen, and the 2003 Tim Burton film Big Fish, the bulk of the film is a series of stories told by an (extremely) unreliable narrator. In the 2006 Tarsem film The Fall, an injured silent-movie stuntman tells heroic fantasy stories to a little girl with a broken arm to pass time in the hospital, which the film visualizes and presents with the stuntman's voice becoming voiceover narration. The fantasy tale bleeds back into and comments on the film's "present-tense" story. There are often incongruities based on the fact that the stuntman is an American and the girl Persian—the stuntman's voiceover refers to "Indians," “a squaw” and “a teepee,” but the visuals show a Bollywood-style devi and a Taj Mahal-like castle.
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Mutations in KIF7 have also been noted in patients that present a similar phenotype to HLS and the characteristic HYLS1 A to G transformation; homozygous deletion of the KIF7 gene causes a variant form of HLS, HLS2. KIF7 encodes a structural factor vital to cilial transport, and is also implicated in other developmental disorders, such as Joubert syndrome (JS). Additionally, mutations in HYLS1 are no longer explicitly connected to HLS in humans. Homozygous mutations removing the stop codon in exon 4 of HYLS1 result in a different genomic sequence disruption to the missense mutation of HLS, and phenotypically present as JS. The ‘molar tooth sign’ of the brain, an anomaly in which cerebellar volume is reduced but cerebellar shape is retained, resembles the molar tooth and is used to identify JS. JS presents with mutations in more than 30 genes, whilst the HYLS1 mutation is the sole cause of HLS, but is also present in the HLS2 variant form with the mutated KIF7 gene.
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Tooth decay There are certain diseases and disorders affecting teeth that may leave an individual at a greater risk for cavities. Molar incisor hypomineralization, which seems to be increasingly common. While the cause is unknown it is thought to be a combination of genetic and environmental factors. Possible contributing factors that have been investigated include systemic factors such as high levels of dioxins or polychlorinated biphenyl (PCB) in the mother's milk, premature birth and oxygen deprivation at birth, and certain disorders during the child's first 3 years such as such as mumps, diphtheria, scarlet fever, measles, hypoparathyroidism, malnutrition, malabsorption, hypovitaminosis D, chronic respiratory diseases, or undiagnosed and untreated coeliac disease, which usually presents with mild or absent gastrointestinal symptoms. Amelogenesis imperfecta, which occurs in between 1 in 718 and 1 in 14,000 individuals, is a disease in which the enamel does not fully form or forms in insufficient amounts and can fall off a tooth.
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Symptoms may consist of the triad of tingling or other skin sensations (paresthesia), tongue soreness (glossitis), and fatigue and general weakness. It presents with a number of further common symptoms, including depressive mood, low-grade fevers, diarrhea, dyspepsia, weight loss, neuropathic pain, jaundice, sores at the corner of the mouth (angular cheilitis), a look of exhaustion with pale and dehydrated or cracked lips and dark circles around the eyes, as well as brittle nails, and thinning and early greying of the hair. Because PA may affect the nervous system, symptoms may also include difficulty in proprioception, memory changes, mild cognitive impairment (including difficulty concentrating and sluggish responses, colloquially referred to as brain fog), and even psychosis, impaired urination, loss of sensation in the feet, unsteady gait, difficulty in walking, muscle weakness and clumsiness. Anemia may also lead to tachycardia (rapid heartbeat), cardiac murmurs, a yellow waxy pallor, altered blood pressure (low or high), and a shortness of breath (known as "the sighs").
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In 2012 he appeared in the ITV series Mrs Biggs with fellow Gavin & Stacey star Sheridan Smith, playing the eponymous character's father Bernard (the real- life father of Charmian Brent, ex-wife of Ronnie Biggs). He played an alien known as Kahler-Jex in an episode of Doctor Who entitled "A Town Called Mercy", which aired on 15 September 2012. On stage, Scarborough has made frequent appearances at the Donmar, the Almeida, and in the West End and he has appeared in twenty productions for the Royal National Theatre. On 19 June 2011, he took part in The Barn Theatre presents... with Elliot Brown at the Barn Theatre, Welwyn Garden City Most recently he has appeared in Hedda Gabler at the Old Vic, again with frequent collaborator Sheridan Smith. In 2013, he played a role in Darkside, Tom Stoppard's radio drama based on Pink Floyd's album The Dark Side of the Moon.
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Moving or touching the limb is often intolerable. With diagnosis of either CRPS types I or II, patients may develop burning pain and allodynia (pain to non-painful stimuli). Both syndromes are also characterized by autonomic dysfunction, which presents with localized temperature changes, cyanosis, and/or edema. The patient may also experience localized swelling; extreme sensitivity to nonpainful stimuli such as wind, water, noise, and vibrations; extreme sensitivity to touch (by themselves, other people, and even their clothing or bedding/blankets); abnormally increased sweating (or absent sweating); changes in skin temperature (alternating between sweaty and cold); changes in skin colouring (from white and mottled to bright red or reddish violet); changes in skin texture (waxy, shiny, thin, tight skin); softening and thinning of bones; joint tenderness or stiffness; changes in nails and hair (delayed or increased growth, brittle nails/hair that easily break); muscle spasms; muscle loss (atrophy); tremors; dystonia; allodynia; hyperalgesia; and decreased/restricted ability and painful movement of affected body part.
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An assortment of cleaning rods used for firearm maintenance: A short cleaning rod with a brass brush attached, a foldable cleaning rod with a nylon brush attached, a cleaning kit for a shotgun (note the thicker rod), and some different brushes. Firearm maintenance (or gun care for short) is a series of periodic preventive maintenance procedures aiming to ensure the proper function of a firearm, often with the use of a variety of specialized tools and chemical solutions. Typically such maintenance is performed by the owner of the firearm using either simple methods such as cleaning the firearm with oil or other cleaning solutions, or more sophisticated practices such as lubricating moving parts with oil/grease and recoating exposed surfaces with protective finishes such as varnishing or bluing. When a firearm presents with physical damage related to the ordinary use of the firearm, or when a firearm malfunctions in a life-threatening manner, a professional gunsmith should perform advanced maintenance to determine if the firearm is repairable and/or safe to shoot anymore.
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Certain medical conditions can cause chronic fatigue and must be ruled out before a diagnosis of CFS can be given. Hypothyroidism, anemia, coeliac disease (that can occur without gastrointestinal symptoms), diabetes and certain psychiatric disorders are a few of the diseases that must be ruled out if the patient presents with appropriate symptoms. Other diseases, listed by the Centers for Disease Control and Prevention, include infectious diseases (such as Epstein–Barr virus, influenza, HIV infection, tuberculosis, Lyme disease), neuroendocrine diseases (such as thyroiditis, Addison's disease, adrenal insufficiency, Cushing's disease), hematologic diseases (such as occult malignancy, lymphoma), rheumatologic diseases (such as fibromyalgia, polymyalgia rheumatica, Sjögren's syndrome, giant-cell arteritis, polymyositis, dermatomyositis), psychiatric diseases (such as bipolar disorder, schizophrenia, delusional disorders, dementia, anorexia/bulimia nervosa), neuropsychologic diseases (such as obstructive sleep apnea, parkinsonism, multiple sclerosis), and others (such as nasal obstruction from allergies, sinusitis, anatomic obstruction, autoimmune diseases, some chronic illness, alcohol or substance abuse, pharmacologic side effects, heavy metal exposure and toxicity, marked body weight fluctuation). Ehlers Danlos syndromes (EDS) may also have similar symptoms.
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Chester Square St Michael's Church, Chester Square Chester Square is an elongated residential garden square in London's Belgravia district. It presents with sister squares: Belgrave and Eaton Squares the garden squares directed to be built by the Grosvenor family when allowing the development of the main part of this semi-rural part of Westminster, being known thenceforth as Belgravia, in the 19th century; the family's trust has retained minor but overarching legal interests in the land, after long-leasing instead of selling as freehold the houses, that is have kept the reversions of most of Belgravia and Mayfair. The square is named after the city of Chester, the market town nearest Eaton Hall, the ancestral home of the Grosvenor family. №32 was used as a backdrop for video accompanying Morrissey's track "Suedehead". The whole except №s 80a, 81, 81a, 82, 83 and 83a (so №s 1–13 and 14–23, 24–32, 37–39, 42–45, 45a, 45b, 65–76 and 77–80, 80a, and 84–88 and the Mews Arch) is listed Grade II for architectural merit.
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Initial diagnosis of HSPs relies upon family history, the presence or absence of additional signs and the exclusion of other nongenetic causes of spasticity, the latter being particular important in sporadic cases. Cerebral and spinal MRI is an important procedure performed in order to rule out other frequent neurological conditions, such as multiple sclerosis, but also to detect associated abnormalities such as cerebellar or corpus callosum atrophy as well as white matter abnormalities. Differential diagnosis of HSP should also exclude spastic diplegia which presents with nearly identical day-to-day effects and even is treatable with similar medicines such as baclofen and orthopedic surgery; at times, these two conditions may look and feel so similar that the only perceived difference may be HSP's hereditary nature versus the explicitly non-hereditary nature of spastic diplegia (however, unlike spastic diplegia and other forms of spastic cerebral palsy, HSP cannot be reliably treated with selective dorsal rhizotomy). Ultimate confirmation of HSP diagnosis can only be provided by carrying out genetic tests targeted towards known genetic mutations.
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He worked with the artist Anthony Benjamin, the singer and tightrope walker Hermine Demoriane, and theatre director Ken Campbell, as well as helping to disguise elephants as mammoths for the film Quest for Fire and co-writing, with Simon Wallace, the music for the Oscar-winning short A Shocking Accident in 1982. In the late 1970s, he began working regularly at the Blitz club in central London, where he met drummer and comedian Rowland Rivron and pianist Rod Melvin. They became the house band at The Comic Strip club, and Brint subsequently wrote several scores for the ensuing TV series, The Comic Strip Presents... With Rivron, he also developed the comedy music act "Raw Sex", in which he performed as the strait-laced father of the dissolute Rivron, most famously on the French and Saunders show. Raw Sex were also the house band on several comedy tours around this time, including Kevin Turvey and the Bastard Squad Featuring The Young Ones, Live, Nigel Planer's Neil's Bad Karma in the UK Tour (with The Wow Show, whose TV series Hello Mum Brint contributed written material to), and French and Saunders' 1990 tour.
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The debate has involved certain insurance industry practices such as the placing of caps on coverage, the high level of co-pays even for essential services such as preventative procedures, the refusal of many insurers to cover pre-existing conditions or adding premium loading for these conditions, and practices which some people regard as egregious such as the additional loading of premiums for women, the regarding of having previously been assaulted by a partner as having a pre-existing condition, and even the cancellation of insurance policies on very flimsy grounds when a claimant who had paid in many premiums presents with a potentially expensive medical condition. Various legislative proposals under serious consideration propose fining larger employers who do not provide a minimum standard of healthcare insurance and mandating that people purchase private healthcare insurance. This is the first time that the Federal government has mandated people to buy insurance, although nearly all states in the union currently mandate the purchase of auto insurance. The legislation also taxes certain very high payout insurance policies (so-called "Cadillac policies") to help finance subsidies for poorer citizens.
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Darkfall has been well received by critics. Eidolon Magazine describes the work as “outstanding in its evocation and control of an invented world and society” and that “her narration presents with equal precision the menace and emotional isolation that threaten her typical victim-heroes”. The Age portray it as a "dramatic narrative [with] vivid characters on an enormous canvas”. InCite praises the work and calls it a "testament to Carmody’s depthless imagination”. She goes on to say that Carmody has avoided the “hackneyed clichés and absolutes common in fantasy novels" and that it "offers believable heroines in a landscape of moral ambiguity”. Magpies magazine says that the “huge cast of characters, events and the intricacies of religion, philosophy and politics keeps readers thinking and puzzling over each chapter”. In the analysis of Foster, Finnis and Nimon, they describe the work as “high fantasy at one level, but on another... a work of social realism, a combination with a variety of different quests and unlikely... heroes”. They also point out the feminist cast of the work, given the protagonists and most of the antagonists are female.
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On January 5, 2020, ASAP Natin' To celebrated its 25th anniversary. In addition, it reverted to its old format and revived some segments that were discontinued after the late 2018 reformat. In 2020, ASAP Natin' To launched a new segment titled ASAP Concert Presents, with the Pair of Aces (Jona Viray and Darren Espanto) performing on the first prod of the segment. In March 2020, ASAP Natin 'To temporarily stopped the admission of the live studio audience as part of the country's fight against the coronavirus. On March 15, 2020, as Metro Manila entered a lockdown, the show stopped live episodes and aired replays for the first 2 weeks, then taped new episodes via work from home arrangements, for the next few weeks. In April 2020, as part of ABS-CBN's temporary programming schedule due to the Luzon Lockdown done to stop the COVID-19 pandemic in the Philippines, in response to rival network GMA extending Kapuso Movie Festival to a two-movie block, which made the network extend the Sunday edition of Kapamilya Blockbusters Family Weekend to two movies, ASAP Natin 'To's airtime was shortened to one hour and moved to Banana Sundae's timeslot of 2:30 pm until May 3, 2020, which was its last airing before indefinite the shutdown of ABS-CBN.
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