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Wolcott-Rallison syndrome

rare

Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure.

Identifiers
MONDO:0009192 OMIM:226980Orphanet:1667
Causal genes
EIF2AK3
Part of
Autosomal recessive diseaseSpondyloepiphyseal dysplasiaSyndromic disease
Also known as
early-onset diabetes mellitus with multiple epiphyseal dysplasia · epiphyseal dysplasia multiple with early-onset diabetes mellitus · IDDM-MED syndrome · MED-IDDM syndrome · Wolcott Rallison syndrome

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