Scapuloperoneal muscular dystrophy (Q41379): Difference between revisions
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Distrofias musculares escapuloperoneais são um grupo de miopatias geneticamente heterogêneas, caracterizadas por fraqueza progressiva e atrofia dos músculos escapulares e anteriores da perna. A distrofia muscular de Emery-Dreifuss é uma distrofia muscular escapuloperoneal clássica associada a contraturas precoces e arritmia cardíaca, mas outros transtornos musculares também podem se apresentar com um fenótipo escapuloperoneal. | |||
| description / en | description / en | ||
Scapuloperoneal muscular dystrophies are a group of genetically heterogeneous myopathies characterised by progressive weakness and wasting of scapular and anterior leg muscles. Emery-Dreifuss muscular dystrophy is a classic scapuloperoneal muscular dystrophy associated with early contractures and cardiac arrhythmia, but other muscle disorders can also present with a scapuloperoneal phenotype. | |||
Revision as of 07:31, 13 August 2026
Scapuloperoneal muscular dystrophies are a group of genetically heterogeneous myopathies characterised by progressive weakness and wasting of scapular and anterior leg muscles. Emery-Dreifuss muscular dystrophy is a classic scapuloperoneal muscular dystrophy associated with early contractures and cardiac arrhythmia, but other muscle disorders can also present with a scapuloperoneal phenotype.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C70.5 |
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| English | Scapuloperoneal muscular dystrophy |
Scapuloperoneal muscular dystrophies are a group of genetically heterogeneous myopathies characterised by progressive weakness and wasting of scapular and anterior leg muscles. Emery-Dreifuss muscular dystrophy is a classic scapuloperoneal muscular dystrophy associated with early contractures and cardiac arrhythmia, but other muscle disorders can also present with a scapuloperoneal phenotype. |
