1993Seminars in NeurologyRequires access

Motor Neuropathy with Multifocal Conduction Block

G. Parry

Open publisher page 36 citations

Abstract

Our present understanding of the syndromes of CIDP and MMN is insufficient to separate them clearly. I believe that MMN is simply a multifocal, predominantly motor variant of CIDP. Furthermore, the highly touted resemblance of MMN to MND has been exaggerated; these syndromes are only superficially similar and can readily be distinguished on clinical and electrophysiologic grounds. MMN is rare but is probably more common than initially believed; certainly, the literature is replete with reports of cases. Further studies are needed to clarify fully the relationship between CIDP and MMN and the role of glycolipid antibodies in MMN and other motor syndromes.

About this research paper

What this paper is about

Our present understanding of the syndromes of CIDP and MMN is insufficient to separate them clearly. I believe that MMN is simply a multifocal, predominantly motor variant of CIDP. Furthermore, the highly touted resemblance of MMN to MND has been exaggerated; these syndromes are only superficially similar and can readily be distinguished on clinical and electrophysiologic grounds. MMN is rare but is probably more common than initially believed; certainly, the literature is replete with reports of cases. Further studies are needed to clarify fully the relationship between CIDP and MMN and the role of glycolipid antibodies in MMN and other motor syndromes.

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OpenAlex reports 36 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Our present understanding of the syndromes of CIDP and MMN is insufficient to separate them clearly. I believe that MMN is simply a multifocal, predominantly motor variant of CIDP. Furthermore, the highly touted resemblance of MMN to MND has been exaggerated; these syndromes are only superficially similar and can readily be distinguished on clinical and electrophysiologic grounds. MMN is rare but is probably more common than initially believed; certainly, the literature is replete with reports of cases. Further studies are needed to clarify fully the relationship between CIDP and MMN and the role of glycolipid antibodies in MMN and other motor syndromes.

Key concepts: Mismatch negativity, Multifocal motor neuropathy, Medicine, Audiology, Neuroscience, Electroencephalography, Psychology, Psychiatry

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