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Wolcott-Rallison syndrome

Disease Export to PDF
Name:
Wolcott-Rallison syndrome
Description:
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.
ORPHAcode:
1667
Synonyms:
Early-onset diabetes mellitus with multiple epiphyseal dysplasia
WRS
XREF(s):
Orphanet
OMIM
MeSH
ICD-10
Analyte(s):
EIF2AK3
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14