Gilbert syndrome - Symptoms & causes - Mayo Clinic
2022年7月1日 · 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: Symptoms, Causes, Tests & Treatment - Cleveland Clinic
2021年1月6日 · 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's syndrome - Wikipedia
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.
Gilbert Syndrome - StatPearls - NCBI Bookshelf
2024年10月5日 · 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: Symptoms, Causes, Diagnosis, and Treatment
2018年9月18日 · 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...
Gilbert's Syndrome - Johns Hopkins Medicine
Gilbert's syndrome is a benign hereditary disease that affects the way bilirubin is processed in the liver and causes jaundice. A blood test can show changes that occur with Gilbert’s syndrome. There is no treatment. However, anyone with jaundice should contact their doctor.
Gilbert syndrome - MedlinePlus
Gilbert syndrome is a relatively mild condition characterized by periods of elevated levels of a toxic substance called bilirubin in the blood (hyperbilirubinemia). Bilirubin, which has an orange-yellow tint, is produced when red blood cells are broken down.
Gilbert Syndrome: Causes, Symptoms, and More - WebMD
2024年11月28日 · 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. When...
Gilbert syndrome - Symptoms, diagnosis and treatment - BMJ …
2024年12月10日 · 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.
Gilbert's syndrome - NHS
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.