Memon Naureen, Weinberger Barry I, Hegyi Thomas, Aleksunes Lauren M
Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Department of Pediatrics, Cohen Children's Medical Center of New York, New Hyde Park, New York.
Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23.
Inherited disorders of hyperbilirubinemia may be caused by increased bilirubin production or decreased bilirubin clearance. Reduced hepatic bilirubin clearance can be due to defective (i) unconjugated bilirubin uptake and intrahepatic storage, (ii) conjugation of glucuronic acid to bilirubin (e.g., Gilbert syndrome, Crigler-Najjar syndrome, Lucey-Driscoll syndrome, breast milk jaundice), (iii) bilirubin excretion into bile (Dubin-Johnson syndrome), or (iv) conjugated bilirubin re-uptake (Rotor syndrome). In this review, the molecular mechanisms and clinical manifestations of these conditions are described, as well as current approaches to diagnosis and therapy.
遗传性高胆红素血症可能由胆红素生成增加或胆红素清除减少引起。肝脏胆红素清除减少可能是由于(i)未结合胆红素摄取及肝内储存缺陷,(ii)胆红素与葡萄糖醛酸结合缺陷(如吉尔伯特综合征、克里格勒 - 纳贾尔综合征、卢西 - 德里斯科尔综合征、母乳性黄疸),(iii)胆红素排泄至胆汁缺陷(杜宾 - 约翰逊综合征),或(iv)结合胆红素重摄取缺陷(罗托综合征)。在本综述中,描述了这些病症的分子机制和临床表现,以及当前的诊断和治疗方法。