Differential diagnosis of chronic dysimmune demyelinating polyneuropathies with and without anti-MAG antibodies.

Abstract:

:The distinction between chronic demyelinating polyneuropathies associated with IgM paraproteinemia and anti-myelin-associated glycoprotein (MAG) antibodies (MAG-PN) and chronic inflammatory demyelinating polyneuropathies (CIDPs) relies on the anti-MAG antibodies assay. The aim of the study was to identify clinical and electrophysiological features suggesting a diagnosis of MAG-PN. Fourteen patients with MAG-PN and 35 with CIDP were included, and a discriminant analysis was performed to identify the clinical and electrophysiological features suggestive of MAG-PN. Pure sensory clinical phenotype, low median and ulnar terminal latency index, and absence of M responses in the lower limbs were significantly associated with the diagnosis of MAG-PN, and indicate a moderate to large increase in probability of this diagnosis in patients with chronic dysimmune demyelinating polyneuropathies.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Isoardo G,Migliaretti G,Ciaramitaro P,Rota E,Poglio F,Tavella A,Paolasso I,Cavallo F,Bergamasco B,Cocito D

doi

10.1002/mus.20230

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

52-8

issue

1

eissn

0148-639X

issn

1097-4598

journal_volume

31

pub_type

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