Αποτελέσματα Αναζήτησης
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.
A panel of clinicians with an interest in liver disease and alcoholic liver disease (ALD), approved by the European Association for the Study of the Liver (EASL) Governing Board, wrote and discussed this Clinical Practice Guidelines (CPG) doc-ument between November 2016 and March 2017.
Gilbert’s syndrome (GS) is a benign hereditary disorder of bilirubin conjugation resulting in an isolated, elevated blood level of unconjugated bilirubin. 1 GS affects 2%–10% of the Caucasian population in the Western world. 2,3 The inheritance pattern for GS is commonly autosomal recessive, but can be dominant as well;
28 Ιαν 2024 · Gilbert's syndrome (GS) is a benign, familial condition characterized by recurrent asymptomatic non-hemolytic low-grade indirect hyper-bilirubinemia.
Gilbert's syndrome is characterised by a mild and intermittent unconjugated hyperbilirubinaemia, with no evidence of haemolysis or liver disease, and with normal liver function tests. It is usually an autosomal recessive disorder and is a common cause of unconjugated hyperbilirubinaemia.
23 Οκτ 2023 · GILBERT SYNDROME OVERVIEW. Gilbert syndrome is an inherited disorder of the liver that results in an overabundance of a substance known as bilirubin. While some people with Gilbert syndrome develop yellowing of the skin or eyes, most people have no symptoms at all.
20 Απρ 2011 · Patients with Gilbert’s syndrome have a defect in the gene that encodes for glucuronyltransferase, which results in a 60-70% reduction in the liver’s ability to conjugate bilirubin.
