Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.
Four members of a family with scapuloperoneal syndrome were examined and investigated. The pattern of inheritance was autosomal dominant and the myopathic basis of the muscle atrophy was established by histological studies of muscle and spinal cord. The family illustrates an unusual combination of f...
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| Publicado no: | J Neurol Neurosurg Psychiatry |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1981
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC491236/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7334411/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.44.12.1146 |
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