Multifocal motor neuropathy: Current concepts and controversies

Research output: Contribution to journalArticle

Abstract

Multifocal motor neuropathy (MMN) is now a well-defined purely motor multineuropathy characterized by the presence of multifocal partial motor conduction blocks (CB), frequent association with anti-GM1 IgM antibodies, and usually a good response to high-dose intravenous immunoglobulin (IVIg) therapy. However, several issues remain to be clarified in the diagnosis, pathogenesis, and therapy of this condition including its nosological position and its relation to other chronic dysimmune neuropathies; the degree of CB necessary for the diagnosis of MMN; the existence of an axonal form of MMN; the pathophysiological basis of CB; the pathogenetic role of antiganglioside antibodies; the mechanism of action of IVIg treatments in MMN and the most effective regimen; and the treatment to be used in unresponsive patients. These issues are addressed in this review of the main clinical, electrophysiological, immunological, and therapeutic features of this neuropathy.

Original languageEnglish
Pages (from-to)663-680
Number of pages18
JournalMuscle and Nerve
Volume31
Issue number6
DOIs
Publication statusPublished - Jun 2005

Keywords

  • Antibodies
  • Axonal excitability
  • Conduction block
  • GM1
  • Intravenous immunoglobulin (IVIg)
  • Multifocal motor neuropathy
  • Therapy

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

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