Population
7 patients with dystrophia myotonica
Comparison
Neurophysiological and histochemical… vs Healthy subjects
Design
Cross-sectional
Authors
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Supports abnormal regeneration in myotonic dystrophy motor units; hypothesis-generating and should not yet change practice.
Patients with dystrophia myotonica exhibit reduced axonal conduction velocity and a reduced proportion of type II motor units in foot extensor muscles, indicating abnormal regeneration or fibre transformation.
Borg et al. (1987) studied this question.
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