Αποτελέσματα Αναζήτησης
1 Ιουλ 2022 · 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 is your largest internal organ.
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 (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]
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'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.
5 Οκτ 2024 · Gilbert syndrome is a benign, inherited disorder of bilirubin metabolism without the risk of progressive liver disease, hepatic decompensation, or increased mortality. However, these patients are at increased risk from drug toxicity when exposed to medications that suppress or affect UGT1A1 activity.
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.
