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Journal of Neurology
Published in: Journal of Neurology 7/2007

Open Access 01-07-2007 | LETTER TO THE EDITORS

Multifocal motor neuropathy with abrupt onset and spontaneous recovery

Authors: C. Bulens, F. H. Vermeij, P. A. van Doorn

Published in: Journal of Neurology | Issue 7/2007

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Excerpt

Sirs: Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness without sensory disturbances, with muscle wasting and fasciculations. It has a slowly, stepwise progressive course. Electrophysiological studies show partial or persistent motor conduction blocks [1]. …
Literature
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Pestronk A, Chaudhry V, Feldman EL, et al. (1990) Lower motor neuron syndromes patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid-antibodies. Ann Neurol 27:316–326CrossRefPubMed
2.
3.
Van Asseldonk JTH, Van den Berg LH, Van den Berg-Vos RM, et al. (2003) Demyelination and axonal loss in multifocal motor neuropathy: distribution and relation to weakness. Brain 126:186–198CrossRefPubMed
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Van Asseldonk JTH, Franssen H, Van den Berg-Vos RM, et al. (2005) Multifocal motor neuropathy. Lancet Neurol 4:309–319CrossRefPubMed
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Chad DA, Hammer K, Sargent J (1986) Slow resolution of multifocal weakness and fasciculation: a reversible motor neuron syndrome. Neurology 36:1260–263PubMed
Metadata
Title
Multifocal motor neuropathy with abrupt onset and spontaneous recovery
Authors
C. Bulens
F. H. Vermeij
P. A. van Doorn
Publication date
01-07-2007
Publisher
Steinkopff-Verlag
Published in
Journal of Neurology / Issue 7/2007
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-006-0413-7

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