Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates

Lancet

Volumn 356, Issue 9230, 2000, Pages 652-653

  Kaplan, M ^a   Hammerman, C ^a   Renbaum, P ^a   Klein, G ^a   Levy Lahad, E ^a  

^a SHAARE ZEDEK MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCURONOSYLTRANSFERASE;

ARTICLE; BLOOD GROUP ABO INCOMPATIBILITY; CONTROLLED STUDY; COOMBS TEST; GENETIC POLYMORPHISM; GILBERT DISEASE; HOMOZYGOTE; HUMAN; HYPERBILIRUBINEMIA; MAJOR CLINICAL STUDY; NEWBORN; PRIORITY JOURNAL; PROMOTER REGION;

EID: 0034686969     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)02610-6     Document Type: Article

References (5)

1. PJ Bosma JR Chowdhury C Bakker The gene basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's Syndrome N Engl J Med 333 1995 1171 1175
2. G Monaghan M Ryan R Seddon R Hume B Burchell Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome Lancet 347 1996 578 581
3. M Kaplan P Renbaum E Levi-Lahad C Hammerman A Lahad E Beutler Gilbert Syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia Proc Natl Acad Sci USA 94 1997 12128 12132
4. A Iolascon MF Faienza A Moretti S Perotta E Miraglia del Giudice UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis Blood 91 1998 1093
5. JD Bancroft B Kreamer GR Gourley Gilbert Syndrome accelerates the development of neonatal jaundice J Pediatr 132 1998 656 660