The clinical features of hereditary motor and sensory neuropathy types I and II.

@article{Harding1980TheCF,
  title={The clinical features of hereditary motor and sensory neuropathy types I and II.},
  author={Anita E. Harding and Professor P. K. Thomas},
  journal={Brain : a journal of neurology},
  year={1980},
  volume={103 2},
  pages={259-80}
}
Observations have been made on a series of 228 patients with hereditary motor and sensory neuropathy, comprising 120 index cases and 108 affected relatives. These could be separated into genetically distinct type I and type II categories depending upon whether motor nerve conduction velocity in the median nerve was below or above 38 m s-1. These disorders constitute separate genetic subgroups within the clinical spectrum of 'peroneal muscular atrophy'. Type I cases were more numerous. Most were… CONTINUE READING
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