A Rare Case Report of Crigler Najjar Syndrome Type II

Crigler-Najjar syndrome is an inborn error of metabolism caused by a point mutation in one of the five exons of UGT1A1 gene, the product of which is responsible for elimination of bilirubin via bile. A number of hyperbilirubinemia disorders similar to Crigler-Najjar syndrome are reported, but they d...

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Detalles Bibliográficos
Autores principales: Abdul Raffay, Eusha, Liaqat, Ayesha, Khan, Maria, Awan, Ali I, Mand, Bakhat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880822/
https://www.ncbi.nlm.nih.gov/pubmed/33604208
http://dx.doi.org/10.7759/cureus.12669

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880822/
https://www.ncbi.nlm.nih.gov/pubmed/33604208
http://dx.doi.org/10.7759/cureus.12669

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