Developing and evaluating a predictive model for neonatal hyperbilirubinemia based on UGT1A1 gene polymorphism and clinical risk factors

Developing and evaluating a predictive model for neonatal hyperbilirubinemia based on UGT1A1 gene polymorphism and clinical risk factors

BackgroundNeonatal hyperbilirubinemia (NHB) is one of the most common diseases in the neonatal period. Without timely diagnosis and treatment, it can lead to long-term complications. In severe cases, it may even result in fatality. The UGT1A1 gene and clinical risk factors play important roles in th...

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Bibliographic Details
Main Authors: Zhaoyang Cui, Wensheng Shen, Xuetong Sun, Yan Li, Ying Liu, Zhiyong Sun
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-02-01
Series:Frontiers in Pediatrics
Subjects:
neonatal hyperbilirubinemia
predictive model
UGT1A1 gene polymorphism
clinical risk factors
transcutaneous bilirubin measurements
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2024.1345602/full

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https://www.frontiersin.org/articles/10.3389/fped.2024.1345602/full

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