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Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine laboratory check-ups or after an intercurrent illness. The diagnosis is typically made per exclusionem, i.e. by excluding other causes of hyperbilirubinaemia.
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.
12 Ιουλ 2023 · Odds ratios for the association between serum bilirubin concentrations, rs887829-T homozygosity (the risk genotype for Gilbert syndrome), genetically predicted bilirubin using rs887829-T allele carriage alone, and a wide range of health outcomes recorded in primary and secondary care. Results.
Diagnosis and Treatment of Alcohol-Associated Liver Diseases: 2019 Practice Guidance From the American Association for the Study of Liver Diseases. Hepatology. 2020 Jan;71 (1):306-333. doi: 10.1002/hep.30866.
Indeed, the the most common causes of abnormal liver blood tests leading to chronic liver disease—namely non-alcoholic fatty liver disease, alcohol-related liver disease and hepatitis C, are frequently associated with only mild or moderate liver blood test abnormalities.
Key learning points. Gilbert’s syndrome (GS) is the commonest hereditary unconjugated hyperbilirubinaemia. GS is a benign, self-resolving jaundice with otherwise normal liver function tests and absence of haemolysis. GS can coexist with other causes of unconjugated hyperbilirubinaemia, in particular hereditary spherocytosis/ thalassaemia.
Gilbert’s syndrome (GS) is a benign genetic disorder that is characterized by intermittent mild jaundice in which the liver doesn’t process bilirubin properly. The aim of this study was to determine whether GS patients have a different personality ...
