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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 a liver condition that can run in families. It is caused by a build-up of bilirubin in your blood. It is a long-term condition that is usually diagnosed in teenagers and young adults. Many people have no symptoms.
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.
Suspect Gilbert's syndrome if a person has: An incidental finding of an increased serum bilirubin concentration, typically not exceeding 68–85 micromol/L, with otherwise normal liver function tests (LFTs).
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. [1]
Jul 13, 2022 · Gilbert's syndrome - also known as constitutional hepatic dysfunction - is a condition where the liver does not process bilirubin very well. It is sometimes called Gilbert's disease although it does not cause 'disease' as such. The liver itself is normal and the condition is harmless.
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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.
