Autoimmune ataxic neuropathies (sensory ganglionopathies).

Abstract:

:Autoimmune ataxic neuropathies are a subset of the sensory ataxic neuropathies which are characterized by ataxia as the dominant presenting feature. The major known causes of autoimmune ataxic neuropathies include sensory variants of the Guillain-Barré syndrome, including Miller-Fisher syndrome, subsets of immunoglobulin M paraproteinaemic neuropathy, paraneoplastic neuropathy and the neuropathy associated with Sjögren's syndrome. Identified antigens as targets for autoantibodies include gangliosides, myelin associated glycoprotein, Hu antigen and extractable nuclear antigens. Some recent studies support the pathogenic role of anti-GD1b ganglioside antibody in autoimmune ataxic neuropathies. The major site of pathology in autoimmune ataxic neuropathies is the dorsal root ganglion, but dorsal roots and peripheral nerve myelin and axons may also be affected.

journal_name

Curr Opin Neurol

authors

O'Leary CP,Willison HJ

doi

10.1097/00019052-199710000-00002

subject

Has Abstract

pub_date

1997-10-01 00:00:00

pages

366-70

issue

5

eissn

1350-7540

issn

1473-6551

journal_volume

10

pub_type

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