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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Autors principals:	Zhaoyang Cui, Wensheng Shen, Xuetong Sun, Yan Li, Ying Liu, Zhiyong Sun
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2024-02-01
Col·lecció:	Frontiers in Pediatrics
Matèries:	neonatal hyperbilirubinemia predictive model UGT1A1 gene polymorphism clinical risk factors transcutaneous bilirubin measurements
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fped.2024.1345602/full
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