Wolcott-Rallison syndrome (Q8029730)
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
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aliases Epiphyseal dysplasia multiple with early-onset diabetes mellitus
WRS
Med-Iddm Syndrome
Early-onset diabetes mellitus with multiple epiphyseal dysplasia
Iddm-Med Syndrome
Wolcott-Rallison Syndrome
Wolcott Rallison syndrome
EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS
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

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