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20 Μαρ 2023 · Gilbert Syndrome is a mild genetic disorder in which the liver does not properly process a substance called bilirubin. Bilirubin is made by the break down of red blood cells. Gilbert Syndrome affects three to seven percent of people in the United States.
6 Ιαν 2021 · Gilbert's syndrome is a genetic liver disease that causes high bilirubin levels. People with Gilbert's syndrome may become jaundiced.
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5 Οκτ 2024 · Gilbert syndrome is a common genetic disorder affecting bilirubin metabolism in the liver. This condition, described in the early 1900s by Gilbert, Castaigne, and Lereboulette, is an autosomal recessive disorder that is a frequent cause of mild-to-moderate isolated unconjugated hyperbilirubinemia.
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.
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Gilbert's syndrome is a diagnosis of exclusion and can be safely and reliably identified in primary care. Normally (allowing for differing laboratory ranges), total bilirubin is less than 17 micromol/L and clinical jaundice becomes apparent at levels over 40 micromol/L.
