Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey

OBJECTIVE: Gilbert syndrome (GS) is a disease characterized by mildly elevated indirect serum bilirubin levels due to mutation in the promoter of the UGT1A1 gene, which causes a decrease in uridine diphosphate glucuronyltransferase enzyme activity. Gilbert syndrome should be considered based on clin...

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Detalles Bibliográficos
Autores principales: Çağan Appak, Yeliz, Aksoy, Betül, Özyılmaz, Berk, Reşid Özdemir, Taha, Baran, Maşallah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Pediatrics Association 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131810/
https://www.ncbi.nlm.nih.gov/pubmed/35781232
http://dx.doi.org/10.5152/TurkArchPediatr.2022.21291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131810/
https://www.ncbi.nlm.nih.gov/pubmed/35781232
http://dx.doi.org/10.5152/TurkArchPediatr.2022.21291

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