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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.
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 a genetic liver disease that causes high bilirubin levels. People with Gilbert's syndrome may become jaundiced.
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, including...
6 Σεπ 2022 · Gilbert syndrome is a mild, nonhemolytic, unconjugated hyperbilirubinemia, defined by bilirubin levels of <6 mg/dL. It is an inherited disorder in which decreased levels of the enzyme uridine-diphosphoglucuronate glucuronosyltransferase (UDPGT) result in impaired conjugation of bilirubin.
Diagnosis is based on higher levels of unconjugated bilirubin in the blood without either signs of other liver problems or red blood cell breakdown. [2][3] Typically no treatment is needed. [1] Gilbert syndrome is associated with decreased cardiovascular health risks. [4]
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.
