Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy

Muscle Nerve. 2000 May;23(5):818-23. doi: 10.1002/(sici)1097-4598(200005)23:5<818::aid-mus23>3.0.co;2-o.

Abstract

A man was identified with two X-chromosomal neuromuscular disorders, X-linked Charcot-Marie-Tooth disease (CMTX) and Becker muscular dystrophy (BMD). The neuropathy could be tracked in the family and was found to be caused by a mutation in the connexin32 gene on Xq13. 1. The muscular dystrophy was sporadic owing to a de novo deletion in the dystrophin gene located in band Xp21.2. Although these genetic alterations of the same X-chromosome are considered as physically independent, their combination resulted in a unique phenotype with severe wasting of proximal as well as distal muscles and rapid progression of both conditions.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Charcot-Marie-Tooth Disease / complications*
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / physiopathology
  • Chromosome Mapping
  • Chromosomes, Human, Pair 17
  • Connexins / genetics*
  • Disease Progression
  • Female
  • Gap Junction beta-1 Protein
  • Genomic Imprinting
  • Humans
  • Male
  • Muscular Dystrophy, Duchenne / complications*
  • Muscular Dystrophy, Duchenne / genetics*
  • Muscular Dystrophy, Duchenne / physiopathology
  • Pedigree
  • X Chromosome*

Substances

  • Connexins