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Article

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

The Libyan journal of medicine - 10 Jun 2013

Habeb Abdelhadi M

Abstract excerpt

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 searched for...

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Identifiers

PMID: 23759358
DOI: 10.3402/ljm.v8i0.21137
PMCID: PMC3679509

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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