Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

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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 WRS in the Kingdom of Saudi Arabia (KSA) based on published data. Methods The Medline database was ...

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ژورنال

عنوان ژورنال: Libyan Journal of Medicine

سال: 2013

ISSN: 1993-2820,1819-6357

DOI: 10.3402/ljm.v8i0.21137