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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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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 (zheel-BAYR) syndrome is a common, harmless liver condition in which the liver doesn't properly process bilirubin. Bilirubin is produced by the breakdown of red blood cells. The liver The liver is your largest internal organ.

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Gilbert's syndrome: Summary. Gilbert's syndrome is an inherited (usually autosomal recessive) metabolic disorder characterized by a mild and intermittent elevation of unconjugated (indirect) bilirubin levels, due to defective conjugating enzymes in the liver. Episodes of jaundice may be precipitated (or exacerbated) by physical or psychological.

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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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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 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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