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Gil bert's syndrome noun. Gil· bert's syndrome. zhēl-ˈberz-: an inherited metabolic disorder characterized by elevated levels of mostly unconjugated serum bilirubin caused especially by defective uptake of bilirubin by the liver. called also Gilbert's disease. Dictionary Entries Near Gilbert's syndrome.
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Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. [1] [2] Reduced glucuronidation of bilirubin leads to unconjugated hyperbilirubinemia and recurrent episodes of jaundice. [1] Under normal circumstances, approximately 95% of bilirubin is unconjugated.
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Gilbert's syndrome is an inherited (genetic) liver disorder that affects the body's ability to process bilirubin. Bilirubin is yellow liquid waste that occurs naturally as the body breaks down old red blood cells. People with Gilbert's syndrome don't produce enough liver enzymes to keep bilirubin at a normal level.
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Gilbert Burns (born July 20, 1986) is a Brazilian professional mixed martial artist, submission grappler and 3rd degree Brazilian jiu-jitsu black belt athlete. [a]
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Gilbert Syndrome sometimes causes the liver to make too much bilirubin that the person becomes jaundiced (yellowing of eyes and skin). Certain things can further increase the level of bilirubin in the bodies of those with Gilbert Syndrome: Being ill. Menstruating. Fasting or skipping meals.
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A single episode (or intermittent episodes) of mild jaundice without clinical evidence of liver disease and associated with physical or psychological stress, including heavy physical exertion, fasting, surgery, dehydration, intercurrent illness, alcohol ingestion, or lack of sleep. To help confirm the diagnosis of Gilbert's syndrome: Ask.
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Gilbert's syndrome is a genetic condition that runs in families. People with the syndrome have a faulty gene, which causes the liver to have problems removing bilirubin from the blood.
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