Population
2 patients with dystrophia myotonica (4 spindles located in extensor indicis biopsies)
Design
Case_series
Authors
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Single-case finding in myotonic dystrophy warrants no practice change; extends histopathology but leaves open functional and clinical relevance.
Electron microscopy reveals severe longitudinal fragmentation of intrafusal muscle fibres and increased satellite cells in patients with dystrophia myotonica.
Stranock et al. (1978) studied this question.
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