Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome

Early-onset diabetes, liver dysfunction, growth retardation, spondyloepiphyseal dysplasia, and tendency to skeletal fractures due to osteopenia are characteristics of Wolcott-Rallison syndrome (WRS). Eukaryotic translation initiation factor 2α kinase (EIF2AK3) is the only known gene, which is respon...

Descripción completa

Detalles Bibliográficos
Autores principales: Behnam, Babak, Shakiba, Marjan, Ahani, Ali, Razzaghy Azar, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759778/
https://www.ncbi.nlm.nih.gov/pubmed/24032041
http://dx.doi.org/10.5812/hepatmon.10124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759778/
https://www.ncbi.nlm.nih.gov/pubmed/24032041
http://dx.doi.org/10.5812/hepatmon.10124

Ejemplares similares