Wolcott-Rallison syndrome (Q86519)
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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 |
||
| 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. |
Statements
CID11:ID_2096915129
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dki-india-ID_2096915129
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Concluído
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13 August 2026
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