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1 Ιουλ 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.
6 Ιαν 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.
18 Σεπ 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 compounds,...
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]
Gilbert's syndrome. In Gilbert's syndrome, slightly higher than normal levels of a substance called bilirubin build up in the blood. Bilirubin is a yellow substance found naturally in the blood. It forms as a by-product when old red blood cells are broken down.
12 Οκτ 2024 · Gilbert syndrome is considered a mild genetic condition affecting the liver, in which the bilirubin levels become elevated in the blood. Bilirubin is a yellow-hued byproduct that forms due to a breakdown of old or worn-out red blood cells. Gilbert syndrome is the most well-known name for this condition, but it may also be referred to as:
6 Σεπ 2022 · Gilbert syndrome (GS) is a genetic syndrome of mild unconjugated hyperbilirubinaemia, by definition <102 micromol/L (<6 mg/dL) (rarely exceeding 68.4 micromol/L [4 mg/dL]). The liver function is otherwise normal. Common syndrome affecting approximately 6% of the general population.
