| Literature DB >> 17242105 |
Christopher Robards1, Sorin J Brull.
Abstract
Crigler-Najjar syndrome is a hereditary condition of unconjugated hyperbilirubinemia due to a deficiency of the enzyme, uridine diphosphate glucuronosyltransferase. Exacerbations of the disease can occur whenever there is either an increase in free serum bilirubin and/or a decrease in serum albumin. The exacerbations can lead to bilirubin encephalopathy and severe brain damage. The goal of anesthetic management in these patients is to prevent an imbalance in the serum bilirubin to serum albumin molar ratio, thereby avoiding neurologic sequelae.Entities:
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Year: 2007 PMID: 17242105 DOI: 10.1213/01.ane.0000252462.70451.0e
Source DB: PubMed Journal: Anesth Analg ISSN: 0003-2999 Impact factor: 5.108