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Liver Transplantation in a Child With Crigler-Najjar Syndrome Type I: A Case Report With Review of the Literature

Crigler-Najjar syndrome (CNS) type I is a rare genetic disease caused by mutations in the UGT1A1 gene, resulting in a lack of Uridine 5'-diphospho-glucuronosyltransferase (UDPGT) enzyme. This enzyme is responsible for the glucuronidation and elimination of unconjugated bilirubin from the body....

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Detalles Bibliográficos
Autores principales:	Alharbi, Faisal A, Al-Shammari, Nawaf R, Aloqeely, Khaled M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2023
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433782/ https://www.ncbi.nlm.nih.gov/pubmed/37602038 http://dx.doi.org/10.7759/cureus.42064

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