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Article

Wolcott-Rallison syndrome.

Orphanet journal of rare diseases - 4 Nov 2010

Julier Cécile, Nicolino Marc

Abstract excerpt

Wolcott-Rallison syndrome (WRS) is a rare autosomal recessive disease, characterized by neonatal/early-onset non-autoimmune insulin-requiring diabetes associated with skeletal dysplasia and growth retardation. Fewer than 60 cases have been described in the literature, although WRS is now recognised as the most frequent cause of neonatal/early-onset diabetes in patients with consanguineous parents. Typically,...

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Identifiers

PMID: 21050479
DOI: 10.1186/1750-1172-5-29
PMCID: PMC2991281

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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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