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.
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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.
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8C70.5
    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.

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