Cap disease (Q90774): Difference between revisions
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Revision as of 17:45, 15 August 2026
Cap disease (also known as Cap myopathy) is a very rare congenital myopathy presenting a weakness of proximal, distal, facial and respiratory muscles associated with craniofacial and thoracic deformities. Onset is at birth or in childhood, weakness progression is slow but may lead to a severe and even fatal prognosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_482118421 |
||
| English | Cap disease |
Cap disease (also known as Cap myopathy) is a very rare congenital myopathy presenting a weakness of proximal, distal, facial and respiratory muscles associated with craniofacial and thoracic deformities. Onset is at birth or in childhood, weakness progression is slow but may lead to a severe and even fatal prognosis. |
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CID11:ID_482118421
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dki-india-ID_482118421
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