| Literature DB >> 26595536 |
Naureen Memon1, Barry I Weinberger2, Thomas Hegyi1, Lauren M Aleksunes3.
Abstract
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.Entities:
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Year: 2015 PMID: 26595536 PMCID: PMC4821713 DOI: 10.1038/pr.2015.247
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756