Multicystic dysplastic kidney: a new association of Wolcott–Rallison syndrome

Wolcott–Rallison syndrome (WRS) is a rare autosomal recessive disorder due to mutations in the EIF2AK3 gene. It is characterized by permanent neonatal diabetes mellitus, skeletal dysplasia, liver impairment, neutropenia and renal dysfunction. Liver is the most commonly affected organ and liver failu...

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Detalles Bibliográficos
Autores principales: Deeb, Asma, Al-Zidgali, Faisal, Ofoegbu, Bibian N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610347/
https://www.ncbi.nlm.nih.gov/pubmed/28955442
http://dx.doi.org/10.1530/EDM-17-0090

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610347/
https://www.ncbi.nlm.nih.gov/pubmed/28955442
http://dx.doi.org/10.1530/EDM-17-0090

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