Category:Wolcott–Rallison syndrome

sindrome di Wolcott-Rallison (it); syndrome de Wolcott-Rallison (fr); Wolcott-Rallison syndrome (en) 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 (en); 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 (it) 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 (en)
Wolcott-Rallison syndrome 
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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Instance ofrare disease,
disease,
developmental defect during embryogenesis
Subclass ofautosomal recessive disease,
developmental anomaly of metabolic origin,
rare diabetes mellitus,
rare genetic diabetes mellitus
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