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Article

Neonatal hyperbilirubinemia and Gilbert's syndrome.

Journal of perinatal medicine - 1 Jan 2002

Laforgia Nicola, Faienza Maria Felicia, Rinaldi Andrea, D'Amato Gabriele, Rinaldi Giuseppe, Iolascon Achille

Abstract excerpt

The role of Gilbert's syndrome (GS) in neonatal hyperbilirubinemia, characterized by bilirubin levels higher than 223 microMol/L during the first seven days of life, has been investigated, evaluating the frequency of GS genotype (A(TA)7TAA polymorphism in the promoter of the gene encoding UGT1). The frequency of GS was significantly higher in the hyperbilirubinemic group, even though neither the peak of...

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Share to Bilirubin
Share to Gilbert Disease
Share to Heterozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

Share to Jaundice, Neonatal

Share to Polymorphism, Genetic

Share to Promoter Regions, Genetic

Source

Identifiers

PMID: 12012638
DOI: 10.1515/JPM.2002.021

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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