[Autosomal recessive forms of Charcot-Marie-Tooth disease]

Bull Acad Natl Med. 2005 Jan;189(1):55-68; discussion 68-9.
[Article in French]

Abstract

In some countries with a high prevalence of consanguineous mariage, autosomal recessive inheritance probably accounts for the vast majority of all forms of CMT. Like dominant forms, autosomal recessive forms are generally subdivided into demyelinating forms (autosomal recessive CMT1: AR-CMT1 or CMT4) and axonal forms (AR-CMT2). Genetic analysis of large families with recessive transmission has identified several novel CMT-related genes (GDAP1, MTMR2, MTMR13, KIAA1985, NDGR1, periaxin and lamin). Given the clinical, electrophysiological and histological heterogeneity of this disease, numerous culprit genes probably remain to be discovered, leading to an even more complex classification. Clinical and histological features often point to the involvement of a particular gene. Nerve biopsy and molecular studies can contribute to the diagnosis, but this approach is highly time-consuming and can only be performed in specialized laboratories.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Charcot-Marie-Tooth Disease / genetics*
  • Humans
  • Mutation
  • Nerve Tissue Proteins / genetics
  • Protein Tyrosine Phosphatases / genetics
  • Protein Tyrosine Phosphatases, Non-Receptor

Substances

  • GDAP protein
  • Nerve Tissue Proteins
  • MTMR2 protein, human
  • Protein Tyrosine Phosphatases
  • Protein Tyrosine Phosphatases, Non-Receptor