Presence of the genetic marker for Gilbert syndrome is associated with increased level and duration of neonatal jaundice
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2002.tb01650.x/fullpdf
Reference5 articles.
1. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferasel in Gilbert's syndrome;Bosma;N Engl J Med,1995
2. Bilirubin metabolism: review and discussion of inborn errors;Valaes;Clin Perinatol,1976
3. Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia;Kaplan;Proc Natl Acad Sci USA,1997
4. UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis;Iolascon;Blood,1998
5. Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn;Monahan;J Pediatr,1999
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