Ataxic Variant of Guillain-Barre Syndrome Associated with Anti-GD1b Ig G Antibody
Journal of the Korean Neurological Association
;
: 269-271, 2004.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Quadriplegia
/
Action Potentials
/
Immunoglobulin G
/
Cerebellar Ataxia
/
Demyelinating Diseases
/
Guillain-Barre Syndrome
/
Eye Movements
/
Neural Conduction
Limits:
Humans
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
2004
Type:
Article
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