Adult onset scapuloperoneal myopathy.
Six cases are described of muscle weakness and wasting of scapuloperoneal distribution with an onset in early adult or middle life and a relatively benign progression. One case also showed mild facial weakness. Four cases were probably sporadic but in two, a mother and daughter, autosomal dominant i...
Uloženo v:
| Vydáno v: | J Neurol Neurosurg Psychiatry |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
1975
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC492137/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1202162/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.38.10.1008 |
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