Category:Wolcott–Rallison syndrome

<nowiki>sindrome di Wolcott-Rallison; syndrome de Wolcott-Rallison; Wolcott–Rallisonin oireyhtymä; Wolcott-Rallison syndrome; متلازمة والكوت راليسون; 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; rara malattia genetica autosomica recessiva caratterizzata principalmente da diabete con esordio neonatale, displasia epifisaria multipla, osteopenia, ritardo mentale o ritardo nello sviluppo e da insufficienza epatica e renale; 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</nowiki>