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What is Gilbert's syndrome?
When was Gilbert syndrome first described?
What are the symptoms of Gilbert syndrome?
Jul 1, 2022 · Gilbert syndrome is caused by a modified gene you inherit from your parents. This gene usually controls an enzyme that helps break down bilirubin in your liver. When you have an ineffective gene, your blood contains excess amounts of bilirubin because your body doesn't produce enough of the enzyme.
Jan 6, 2021 · 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.
Gilbert syndrome produces an elevated level of unconjugated bilirubin in the bloodstream, but normally has no consequences. Mild jaundice may appear under conditions of exertion, stress, fasting, and infections, but the condition is otherwise usually asymptomatic.
Feb 6, 2023 · 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.
- 2023/02/06
Feb 9, 2018 · Gilbert’s syndrome is an inherited liver condition in which your liver can’t fully process a compound called bilirubin. Your liver breaks down old red blood cells into...
Aug 28, 2022 · What Is Gilbert’s Syndrome? Gilbert’s syndrome (also called constitutional hepatic dysfunction or familial nonhemolytic jaundice) is a common disorder that's passed through families.
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.
