Literature DB >> 1469432

Multifocal motor nerve conduction abnormalities in amyotrophic lateral sclerosis.

I Wirguin1, T Brenner, Z Argov, I Steiner.   

Abstract

Motor nerve conduction in motor neuron disease is considered normal until the terminal stages of the disease, a notable exception being lower motor neuron syndrome associated with anti-glycolipid antibodies. We reviewed the electrophysiological findings in all our patients who were diagnosed as having amyotrophic lateral sclerosis (ALS) during the last 6 years. Six patients, clinically indistinguishable from "classical" ALS patients, out of 31 (19%) displayed motor nerve conduction abnormalities. The most consistent finding, occurring in all 6, was prolonged distal latency or reduced conduction velocity in the distal segment of the median nerve, with normal sensory conduction, suggesting possible pressure proneness of motor nerve fibers in ALS. Additional abnormalities included multifocal motor conduction slowing (3 patients), and conduction blocks (4 patients). None of the patients had paraproteinemia and anti-GM1 and anti-GD1a antibodies were not detected. Thus, a subgroup of clinically indistinguishable ALS patients may have multifocal motor nerve conduction abnormalities, indicating motor nerve fiber involvement. The etiology and pathogenesis of the peripheral nerve involvement are presently unknown.

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Year:  1992        PMID: 1469432     DOI: 10.1016/0022-510x(92)90151-a

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  3 in total

Review 1.  Immunological findings in amyotrophic lateral sclerosis.

Authors:  J P Antel; N R Cashman
Journal:  Springer Semin Immunopathol       Date:  1995

2.  Familial inflammatory demyelinating polyneuropathy: a Guillain-Barré syndrome variant without autoimmune predilection.

Authors:  I Korn-Lubetzki; I Steiner; T Brenner; C Brautbar; Z Argov
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-08       Impact factor: 10.154

3.  Electrophysiological and spinal imaging evidences for sensory dysfunction in amyotrophic lateral sclerosis.

Authors:  Caroline Iglesias; Sina Sangari; Mohamed-Mounir El Mendili; Habib Benali; Véronique Marchand-Pauvert; Pierre-François Pradat
Journal:  BMJ Open       Date:  2015-02-24       Impact factor: 2.692

  3 in total

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