Autonomic and respiratory dysfunction in Charcot-Marie-Tooth disease due to Thr124Met mutation in the myelin protein zero gene

Clin Neurophysiol. 2003 Sep;114(9):1609-14. doi: 10.1016/s1388-2457(03)00159-7.

Abstract

Objective: To report the clinical and electrophysiological characteristics of a family presenting Charcot-Marie-Tooth disease (CMT) associated with autonomic nervous system disturbances.

Methods: We studied nerve conduction values, postural adaptation, sympathetic skin reflex, the variation in heart rate by the Valsalva ratio and pupillometry in 7 members of a French family in which CMT due to a Thr124Met mutation in the myelin protein zero (MPZ) gene was diagnosed.

Results: Clinical and laboratory evidence of autonomic nervous system disturbances were found in the affected individuals. The clinical phenotype was characterized by sensorimotor peripheral neuropathy, defined as axonal type by electrophysiological studies, and was associated with severe pain, bladder dysfunction, sudorimotor disturbances and abolished pupillary reflex to light. Moreover, two patients had severe restrictive respiratory insufficiency requiring noninvasive mechanical ventilation.

Conclusions: Our study demonstrates that autonomic disturbances may be one of the major clinical signs associated with CMT secondary to MPZ gene mutation in codon 124. Testing of pupillary reflex allows the discrimination of affected and unaffected subjects in our family. However, involvement of the autonomic nervous system in this type of neuropathy is unclear and further studies are required to elucidate the role of the MPZ gene in the autonomic nervous system.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Autonomic Nervous System Diseases / complications
  • Autonomic Nervous System Diseases / genetics*
  • Charcot-Marie-Tooth Disease / complications
  • Charcot-Marie-Tooth Disease / genetics*
  • DNA Mutational Analysis
  • Evoked Potentials / physiology
  • Family Health
  • Female
  • France
  • Genetic Linkage
  • Humans
  • Male
  • Methionine / genetics*
  • Middle Aged
  • Muscles / physiology
  • Myelin P0 Protein / genetics*
  • Neural Conduction / physiology
  • Point Mutation*
  • Polymerase Chain Reaction / methods
  • Pupil / physiology
  • Respiration Disorders
  • Respiratory Tract Diseases
  • Threonine / genetics*
  • Urinary Bladder / physiology

Substances

  • Myelin P0 Protein
  • Threonine
  • Methionine