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Article

Gilbert syndrome accelerates development of neonatal jaundice.

The Journal of pediatrics - 1 Apr 1998

Bancroft J D, Kreamer B, Gourley G R

Abstract excerpt

OBJECTIVE: Gilbert Syndrome (GS), associated with unconjugated hyperbilirubinemia and decreased bilirubin UDP-glucuronosyltransferase activity, is usually diagnosed after puberty. The role of GS in neonatal jaundice is unknown. This study tested the hypothesis that a recently identified molecular marker for GS (a TA insertion in the promoter of UGT1A, the gene encoding bilirubin UDP-glucuronosyltransferase) is...

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Share to Genetic Markers
Share to Glucuronosyltransferase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9580766
DOI: 10.1016/s0022-3476(98)70356-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Gilbert syndrome accelerates development of neonatal jaundice.PMID 9580766Read ↗

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Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.Semantic proximity Read ↗

Presence of the genetic marker for Gilbert syndrome is associated with increased level and duration of neonatal jaundiceSemantic proximity Read ↗

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.Semantic proximity Read ↗

Gilbert’s syndrome: High frequency of the (TA)7TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 geneSemantic proximity Read ↗

Neonatal jaundice and bilirubin UDP-glucuronosyl transferase 1A1 gene polymorphism in Turkish patients.Semantic proximity Read ↗

UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.Semantic proximity Read ↗

Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.Semantic proximity Read ↗

A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.Semantic proximity Read ↗

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.Semantic proximity Read ↗

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