Novel Mutation in Wolcott–Rallison Syndrome with Variable Expression in Two Omani Siblings

Wolcott-Rallison syndrome (WRS) is an autosomal recessive disease, characterized by neonatal or early-onset non-autoimmune insulin-dependent diabetes. WRS, although rare, is recognized to be the most frequent cause of neonatal-onset diabetes. The majority of reported patients are from consanguineous...

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Detalhes bibliográficos
Publicado no:Oman Med J
Main Authors: Al-Sinani, Siham, Al-Yaarubi, Saif, Sharef, Sharef Waadallah, Al-Murshedi, Fathyia, Al-Maamari, Watfa
Formato: Artigo
Idioma:Inglês
Publicado em: OMJ 2015
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4412448/
https://ncbi.nlm.nih.gov/pubmed/25960841
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2015.29
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