Correlation of UGT1A1 genotypes with newborn hyperbilirubinemia using newborn genetic screening

BackgroundThis study evaluated whether uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) variants identified through newborn genetic screening are associated with the development of clinically significant neonatal hyperbilirubinemia.MethodsNext-generation sequencing (NGS) was performed in 1,0...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Qianyong Ji, Wen Zeng, XiaoOu Li, ShukChing Chong, JianJiang Zhu
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2026-07-01
coleção:	Frontiers in Pediatrics
Assuntos:	bilirubin newborn newborn genetic screening newborn hyperbilirubinemia UGT1A1 gene
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fped.2026.1737797/full
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!