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PMID: 1381168 Published · ppublish English Case Reports Journal Article

Sensory neuropathy associated with monoclonal immunoglobulin M to GD1b ganglioside.

Annals of neurology ·Vol. 31 ·No. 6 ·1992-06-00 ·Pages 683-5

Daune GC, Farrer RG, Dalakas MC, Quarles RH

Abstract

A 67-year-old woman with a sensory polyneuropathy was shown to have a serum monoclonal immunoglobulin M lambda antibody with a titer of 1:10,000 toward GD1b ganglioside. The immunoglobulin M also reacted with some other gangliosides containing disialosyl groups such as GD2, GD3, and GQ1b, but it did not react with GM1, LM1, or GD1a. The principal reactive ganglioside in human cauda equina was GD1b.

MeSH Terms
Aged Antibodies, Monoclonal/immunology Autoantibodies/immunology Autoimmune Diseases/etiology,immunology Cauda Equina/immunology Epitopes/immunology Extremities Female Gangliosides/immunology Humans Hypesthesia/etiology,immunology Immunoglobulin M/immunology Monoclonal Gammopathy of Undetermined Significance/complications,immunology Paresthesia/etiology,immunology Peripheral Nerves/immunology
Chemicals
Antibodies, Monoclonal Autoantibodies Epitopes Gangliosides Immunoglobulin M ganglioside, GD1b
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Daune G C
Myelin and Brain Development Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
Farrer R G
Dalakas M C
Quarles R H
Article Info
Journal
Annals of neurology
Abbr.
Ann Neurol
ISSN
0364-5134
Published
1992-06-00
Pages
683-5
Language
English
Region
United States
NLM ID
7707449
Subset
IM
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