Gilbert综合征又称特发性结合性胆红素血症,是由于肝组织摄取非结合胆红素障碍或微粒体内葡萄糖醛酸转移酶(UGT)不足,致使血液中非结合胆红素显著增高而发生黄疸的一类常染色体显性遗传性疾病,好发于青壮年。在临床上诊断时程较长,且易误诊为各种肝炎[1],常导致不必要的医疗费? Gilbert syndrome, also known as idiopathic combined bilirubin, is due to liver tissue uptake of unconjugated bilirubin or microsomal in vivo glucuronosyltransferase (UGT) deficiency, resulting in a significant increase in blood unconjugated bilirubin Occurrence of jaundice and a class of autosomal dominant genetic disease occurs in young adults. In the clinical diagnosis of longer duration, and often misdiagnosed as a variety of hepatitis [1], often lead to unnecessary medical expenses?