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Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome Project.

Tiantian XiaoJin WangHuijun WangHongfang MeiXinran DongYulan LuGuoqiang ChengLaishuan WangLi-Yuan HuWei LuQi NiGang LiPing ZhangYanyan QianXu LiXiaomin PengYao WangChun ShenGong ChenYa-Lan DouYun CaoLiping ChenWenqing KangLong LiXinnian PanQiufen WeiDeyi ZhuangDong-Mei ChenZhaoqing YinJianshe WangLin YangBingbing WuWen-Hao Zhou
Published in: Archives of disease in childhood. Fetal and neonatal edition (2022)
Known aetiologies were identified in approximately 80% of neonates in our cohort, and their overall outcomes were favourable. Genetic aetiology should be considered a priority in neonates with PCHB or the persistence of jaundice after 4 weeks of age. Moreover, genetic data can modify the clinical diagnosis and guide disease management, potentially improving outcomes.
Keyphrases
  • genome wide
  • electronic health record
  • low birth weight
  • gene expression
  • quality improvement
  • dna methylation
  • preterm infants
  • data analysis