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Many people never have symptoms. [1] Occasionally jaundice (a slight yellowish color of the skin or whites of the eyes) may occur. [1] Gilbert syndrome is due to a genetic variant in the UGT1A1 gene which results in decreased activity of the bilirubin uridine diphosphate glucuronosyltransferase enzyme.
obstructive jaundice: palpable gall bladder w/ painless jaundice unlikely to be cholelithiasis Crichton-Browne sign: Sir James Crichton-Browne: neuropsychiatry 'general paresis' tremor at corners of mouth and of outer canthus Crowe sign: Frank W. Crowe: dermatology: neurofibromatosis type I: axillary freckling Cruveilhier–Baumgarten bruit
With his former trainee and colleague Michel Odièvre, he wrote the first textbook of pediatric hepatology, Maladies du Foie et des Voies Biliaires chez l'Enfant (Liver and Bile Duct Diseases in Children). [2] In 1994, he became the third recipient of the Andrew Sass Kortsak Award from the Canadian Liver Foundation. [6]
[1] [2] Patients observe these symptoms and seek medical advice from healthcare professionals. Because most people are not diagnostically trained or knowledgeable, they typically describe their symptoms in layman's terms, rather than using specific medical terminology. This list is not exhaustive.
The severity of the disorder can vary within the same family, with symptoms ranging from so mild as to go unnoticed, to severe heart and/or liver disease that requires transplantation. [6] It is uncommon, but Alagille syndrome can be a life-threatening disease with a mortality rate of 10%. [ 7 ]
Image credits: Michael Buckner / Getty #3 Scott Disick. Boxes of Mounjaro, which is known for its weight loss effects, were found stacked in Scott Disick’s fridge on a past episode of The ...
Jaundice, also known as icterus, is a yellowish or greenish pigmentation of the skin and sclera due to high bilirubin levels. [3] [6] Jaundice in adults is typically a sign indicating the presence of underlying diseases involving abnormal heme metabolism, liver dysfunction, or biliary-tract obstruction. [7]
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...