Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy

Ted M. Burns, Lawrence H. Phillips, Elliot L. Dimberg, Barry K. Vaught, Christopher J. Klein

Research output: Contribution to journalArticle

12 Scopus citations

Abstract

We present a patient with acute onset painful polyneuropathy found to have a novel MPZ mutation (Arg36Trp). The Arg36Trp mutation described in this report occurs at a putative adhesion interface. An alternative explanation for his polyneuropathy was not found and his mother was identified to have polyneuropathy and carry the same mutation. Two hundred normal controls were without this base alteration. The temporal profile of the index case may provide further indirect evidence suggesting an immune mechanism contributing to the pathogenesis of some cases of MPZ mutations. We predict that other rapid symptom onset polyneuropathies will be found to have direct genetic susceptibility.

Original languageEnglish (US)
Pages (from-to)308-310
Number of pages3
JournalNeuromuscular Disorders
Volume16
Issue number5
DOIs
StatePublished - May 1 2006

Keywords

  • Charcot-Marie-Tooth disease
  • Hereditary motor and sensory neuropathy
  • MPZ mutation

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Neurology
  • Clinical Neurology
  • Genetics(clinical)

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