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 s...
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| Format: | Article |
| Language: | English |
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Taylor & Francis Group
2013-06-01
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| Series: | Libyan Journal of Medicine |
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| Online Access: | http://www.libyanjournalofmedicine.net/index.php/ljm/article/download/21137/pdf_1 |