We report the case of a 24 year old woman who developed myasthenia gravis in the course of a mild form of Charcot-Marie-Tooth neuropathy. We describe the clinical manifestations together with the neurophysiological, pathological, serological findings and response to therapy and discuss the unusual association in the light of the relevant literature. © 1992 Masson Italia Periodici S.r.l.
|Number of pages||3|
|Journal||Italian Journal of Neurological Sciences|
|Publication status||Published - 1992|
All Science Journal Classification (ASJC) codes
- General Neuroscience
- Clinical Neurology