Hereditary distal myopathy with filamentous inclusions
- 1 April 1982
- journal article
- case report
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 65 (4), 363-368
- https://doi.org/10.1111/j.1600-0404.1982.tb03093.x
Abstract
A 25‐year‐old man and his sister aged 30 were thought to have autosomal recessive distal myopathy. Muscle biopsies showed myopathic changes with prominent vacuoles, basophilic granular material and eosinophilic bodies. Electron microscopy revealed collections of sarcoplasmic filamentous inclusions 15–20 nm wide.Keywords
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