Wolcott-Rallison syndrome (Q86519): Difference between revisions
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A síndrome de Wolcott-Rallison (WRS) é uma doença genética muito rara, caracterizada por diabetes mellitus neonatal permanente, displasia epifisária múltipla e outras manifestações clínicas, incluindo episódios recorrentes de insuficiência hepática aguda. | |||
| description / en | description / en | ||
Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterised by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure. | |||
Revision as of 11:56, 15 August 2026
Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterised by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2096915129 |
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| English | Wolcott-Rallison syndrome |
Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterised by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure. |
