Charcot-Marie-Tooth Disease Associated with ‘Essential Tremor’ and Normal and/or Slightly Diminished Motor Conduction Velocity
- 1 January 1979
- journal article
- research article
- Published by S. Karger AG in European Neurology
- Vol. 18 (1) , 49-58
- https://doi.org/10.1159/000115053
Abstract
A study of 7 patients with Charcot-Marie-Tooth disease, associated with a dyskinesia clinically identical with essential tremor, in which motor conduction velocity in the upper limbs was normal or slightly diminished was presented. An analysis of age of onset, sex distribution and clinicals signs from cases in the literature is compared with the present series. A family with Charcot-Marie-Tooth disease in which affected members have widely different motor conduction velocity values is reported. Stress is laid upon the fact that categorization of this disease on electrophysiological studies in the upper limbs may present considerable difficulties.This publication has 6 references indexed in Scilit:
- The peroneal muscular atrophy syndromeJournal of the Neurological Sciences, 1977
- The peroneal muscular atrophy syndromeJournal of the Neurological Sciences, 1977
- Argyll-Robertson-Like Pupils in the Neural Type of Charcot-Marie-Tooth DiseaseEuropean Neurology, 1977
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968
- Lower Motor and Primary Sensory Neuron Diseases With Peroneal Muscular AtrophyArchives of Neurology, 1968
- OBSERVATIONS ON ESSENTIAL (HEREDOFAMILIAL) TREMORBrain, 1949