Ataxic Variant of Guillain-Barre Syndrome Associated with Anti-GD1b Ig G Antibody
Journal of the Korean Neurological Association
;
: 269-271, 2004.
Article
Dans Coréen
| WPRIM
| ID: wpr-204335
ABSTRACT
It is known that anti GD1b antibody bind to the cerebellar granular layer or spinocerebellar Ia fiber. We recently encountered a patient of Guillain Barr syndrome (GBS) showing marked cerebellar ataxia and relatively mild quadriparesis but completely intact extraocular eye movement. Markedly high IgG anti GD1b antibody titer was identified from the patient's serum. The nerve conduction study showed reduction of compound muscle action potential without evidence of perpheral nerve demyelination. We report an ataxic variat of GBS associated with anti GD1b IgG antibody.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Tétraplégie
/
Potentiels d'action
/
Immunoglobuline G
/
Ataxie cérébelleuse
/
Maladies démyélinisantes
/
Syndrome de Guillain-Barré
/
Mouvements oculaires
/
Conduction nerveuse
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Neurological Association
Année:
2004
Type:
Article
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