Spinal Charcot-Marie-Tooth disease: a reappraisal

Muscle Nerve. 2012 Oct;46(4):604-9. doi: 10.1002/mus.23456.

Abstract

Introduction: Distal hereditary motor neuropathy (dHMN) is characterized by isolated distal muscle atrophy without sensory deficit. Nevertheless, clinical sensory loss has been reported despite preserved sensory nerve conduction in a few patients, thus differentiating these cases from the classical type 2 Charcot-Marie-Tooth disease (CMT2).

Methods: We report 4 patients who presented with clinical sensory and motor neuropathy and normal peripheral sensory nerve conduction studies and were investigated with complete electrophysiological studies, including somatosensory evoked potentials (SEP).

Results: These patients had a clinical presentation of classical CMT with isolated axonal motor neuropathy suggestive of dHMN. Interestingly, tibial nerve SEPs showed abnormalities suggestive of proximal involvement of dorsal roots that may explain the clinical somatosensory disturbances.

Conclusions: These cases support the concept of spinal CMT that should be recognized as an intermediate form between dHMN and CMT2. SEP recording was helpful in defining a more precise phenotype of spinal CMT.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Aged
  • Charcot-Marie-Tooth Disease / classification
  • Charcot-Marie-Tooth Disease / diagnosis*
  • Charcot-Marie-Tooth Disease / physiopathology*
  • Diagnosis, Differential
  • Female
  • Humans
  • Male
  • Spinal Diseases / classification
  • Spinal Diseases / diagnosis*
  • Spinal Diseases / physiopathology*