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Multifocal demyelinating neuropathy with persistent conduction block

Lewis, Richard A., Sumner, Austin J., Brown, Mark J., Asbury, Arthur K.·1982·Neurology

Abstract

We describe five patients with a chronic asymmetric sensorimotor neuropathy most pronounced in the upper extremities with focal involvement of individual nerves. Diagnosis was established by electrophysiologic evidence of persistent multifocal conduction block. Sural nerve biopsy in three patients showed primarily demyelinating-remyelinating changes with varying degrees of fiber loss. Two patients had acute optic neuritis, indicating that the disorder was not always restricted to the peripheral nervous system. Two patients treated with corticosteroids improved, whereas three untreated patients had static deficits or steady progression of symptoms. Chronic multifocal demyelinating neuropathy with persistent conduction block seems to be a variant of chronic acquired demyelinating polyneuropathy and may be immunologically mediated.

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Metadata

Authors
Lewis, R. A., Sumner, A. J., Brown, M. J., & Asbury, A. K.
Venue
Neurology
Published
1982-09
Volume
32
Issue
9
Pages
958-958
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2014464814
Cited by
502
References
0
FWCI
2.13
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Multifocal demyelinating neuropathy with persistent conduction block. https://app.cochat.ai/papers/10.1212/wnl.32.9.958
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Lewis, R. A., Sumner, A. J., Brown, M. J., & Asbury, A. K. (1982). Multifocal demyelinating neuropathy with persistent conduction block. Neurology. https://doi.org/10.1212/wnl.32.9.958

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.