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Gilbert syndrome (GS) is a syndrome in which the liver of affected individuals processes bilirubin more slowly than the majority. [1] Many people never have symptoms. [ 1 ] Occasionally jaundice (a slight yellowish color of the skin or whites of the eyes) may occur.
Gilbert Syndrome, a hereditary disease affecting 5% of the US population, leads to stress-induced mild hyperbilirubinemia. [9] The mutated UGT1 gene produces defective UGT1A1 enzymes vital for bilirubin conjugation.
Crigler-Najjar syndrome is much more severe and presents in newborns. Crigler-Najjar syndrome is the complete or near complete inactivity absence of UGT1A1 activity a more severe unconjugated hyperbilirubinemia compared to Gilbert Syndrome. [2] Dubin-Johnson syndrome and Rotor syndrome cause elevations in conjugated bilirubin. These conditions ...
Gilbert's syndrome; Gulf War syndrome; H. Haber syndrome; Hagemoser–Weinstein–Bresnick syndrome; ... Sudden infant death syndrome; Sudden wealth syndrome;
Kernicterus is a bilirubin-induced brain dysfunction. [1] The term was coined in 1904 by Christian Georg Schmorl.Bilirubin is a naturally occurring substance in the body of humans and many other animals, but it is neurotoxic when its concentration in the blood is too high, a condition known as hyperbilirubinemia.
Gilbert Gottfried's death was caused by an illness called ventricular tachycardia due to myotonic dystrophy, a type of muscular dystrophy.
UGT1A1, UGT1A6, and UGT1A7 (enzymes deficient in most people with Gilbert's syndrome) deal with much more than just bilirubin. This wiki page is outdated and inaccurate because it fails to mention what other substances the enzymes process and the effects of their deficiency in people with Gilbert's syndrome, theoretically speaking.
Gilbert's syndrome – a genetic disorder of bilirubin metabolism that can result in mild jaundice, found in about 5% of the population; Rotor syndrome: non-itching jaundice, with rise of bilirubin in the patient's serum, mainly of the conjugated type; Dubin–Johnson syndrome; Crigler–Najjar syndrome