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Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review
BACKGROUND: Wolcott–Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis. The frequency of this rare syndrome is largely unknown. OBJECTIVES: To define the frequency and spectrum of...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Co-Action Publishing
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679509/ https://www.ncbi.nlm.nih.gov/pubmed/23759358 http://dx.doi.org/10.3402/ljm.v8i0.21137 |