Cap disease (Q90774): Difference between revisions
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A doença de Cap (também conhecida como miopatia de Cap) é uma miopatia congênita muito rara que apresenta uma fraqueza dos músculos proximais, distais, faciais e respiratórios associada a deformidades craniofaciais e torácicas. O início é ao nascimento ou na infância, a progressão da fraqueza é lenta, mas pode levar a um prognóstico grave e até fatal. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
