Rapidly progressive, predominantly motor Guillain-Barré syndrome with anti-GalNAc-GD1a antibodies

To investigate the presence of anti-GalNAc-GD1a antibodies in patients with Guillain-Barré syndrome (GBS) and to determine the relation of anti-ganglioside antibodies with clinical features. The GBS is heterogeneous with regard to clinical manifestations, antecedent infections, and the presence and...

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Veröffentlicht in:Neurology 1999-12, Vol.53 (9), p.2122-2127
Hauptverfasser: ANG, C. W, YUKI, N, JACOBS, B. C, KOGA, M, VAN DOORN, P. A, SCHMITZ, P. I. M, VAN DER MECHE, F. G. A
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Sprache:eng
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Zusammenfassung:To investigate the presence of anti-GalNAc-GD1a antibodies in patients with Guillain-Barré syndrome (GBS) and to determine the relation of anti-ganglioside antibodies with clinical features. The GBS is heterogeneous with regard to clinical manifestations, antecedent infections, and the presence and specificity of anti-ganglioside antibodies. Recently, antibodies to minor gangliosides have been identified in serum from GBS patients. The authors used ELISA to detect anti-ganglioside antibodies in 132 GBS patients and then correlated results with a database containing information on antecedent infections and clinical parameters. Anti-GalNAc-GD1a antibodies could be detected in 19 (14%) GBS patients. The presence of anti-GalNAc-GD1a antibodies was related to antecedent Campylobacter jejuni infection (p
ISSN:0028-3878
1526-632X
DOI:10.1212/WNL.53.9.2122