UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice

UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice

BackgroundThis study aimed to investigate the influence of a variant of the UGT1A1 gene on the occurrence and severity of prolonged jaundice in Chinese infants at term.Methods175 infants with prolonged jaundice and 149 controls were used in this retrospective case-control study. The infants with pro...

Full description

Bibliographic Details
Main Authors: Zhe Yang, Fen Lin, Jia-Xin Xu, Hui Yang, Yong-Hao Wu, Zi-Kai Chen, He Xie, Bin Huang, Wei-Hao Lin, Jian-Peng Wu, Yu-Bin Ma, Jian-Dong Li, Li-Ye Yang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Pediatrics
Subjects:
UGT1A1
prolonged jaundice
G6PD deficiency
breast feeding
neonatal hyperbilirubinemia
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2022.1080212/full

Internet

https://www.frontiersin.org/articles/10.3389/fped.2022.1080212/full

Similar Items