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Article

Wolcott-Rallison syndrome: a case series of three patients.

Pediatric endocrinology, diabetes, and metabolism - 1 Jan 2022

Memon Fozia, Arif Muzna, Kirmani Salman, Humayun Khadija

Abstract excerpt

INTRODUCTION: Neonatal diabetes is a rare disease with incidence estimated at 1 in 300,000 to 1 in 400,000 live births. Walcott-Rallison syndrome has been identified as the most common cause of permanent neonatal diabetes in consanguineous families caused by mutations in eukaryotic translation initiation factor 2-α kinase 3 (EIF2AK3), characterized by permanent neonatal diabetes associated with liver dysfunction,...

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Identifiers

PMID: 36106422
DOI: 10.5114/pedm.2022.118325
PMCID: PMC10214929

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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