Cargando…
Wolcott-Rallison syndrome
Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation. Fewer than 60 cases have been described in the literature, although WRS is now recognised...
Autores principales: | Julier, Cécile, Nicolino, Marc |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991281/ https://www.ncbi.nlm.nih.gov/pubmed/21050479 http://dx.doi.org/10.1186/1750-1172-5-29 |
Ejemplares similares
-
Wolcott-Rallison syndrome in a Bedouin boy
por: Marafie, Makia J., et al.
Publicado: (2004) -
Neonatal diabetes in Wolcott–Rallison syndrome: a case report
por: Ngoc, Can Thi Bich, et al.
Publicado: (2013) -
Ketoacidosis in Neonatal Diabetes Mellitus, Part of Wolcott-Rallison Syndrome
por: Sreeramaneni, Poorna Gopal Azad, et al.
Publicado: (2017) -
Wolcott-Rallison syndrome: a case series of three patients
por: Memon, Fozia, et al.
Publicado: (2022) -
Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review
por: Habeb, Abdelhadi M.
Publicado: (2013)