Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2

Ritsuko Yoshioka, Peter James Dyck, Phillip F. Chance

Research output: Contribution to journalArticle

44 Scopus citations

Abstract

Charcot-Marie-Tooth neuropathy type 2 (CMT2) is a common inherited axonal neuropathy. The locus for one form of CMT2 (CMT2A) is assigned to the short arm of chromosome 1. There is genetic heterogeneity in CMT2 because additional pedigrees do not demonstrate linkage to chromosome 1 and are designated as CMT2B. Further clinical heterogeneity is suggested by CMT2 pedigrees with diaphragm and vocal cord weakness and are designated as CMT2C. To address the possible genetic distinction between CMT2A and CMT2C, we tested markers from the CMT2A locus for linkage in a large CMT2C pedigree. There was no evidence to support linkage of the CMT2C gene to the region of the CMT2A locus on chromosome 1. CMT2C is not an allelic variant of CMT2A. This analysis provides further evidence for genetic heterogeneity within inherited axonal neuropathies.

Original languageEnglish (US)
Pages (from-to)569-571
Number of pages3
JournalNeurology
Volume46
Issue number2
DOIs
StatePublished - Feb 1996

ASJC Scopus subject areas

  • Clinical Neurology

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