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Published on: September 26, 2012
Cerebellar ataxia and autoantibodies restricted to glutamic acid decarboxylase 67 (GAD67)
Mar Guasp1, Nuria Solà-Valls1, Eugenia Martínez-Hernández2
1Service of Neurology, Hospital Clínic, Universitat de Barcelona, Barcelona, Spain.
Abstract:
Cerebellar ataxia is one of the most frequent syndromes associated with autoantibodies against glutamic acid decarboxylase (GAD-ab). Antibodies recognize the isoform GAD65, which is the standard biomarker, but additional immunoreactivity against GAD67 is found in high proportion of patients with GAD-ab-associated neurological disorders. We describe the case of a 59-year-old woman who presented with pancerebellar syndrome of subacute onset (9weeks to nadir). In the etiological study, high titers of GAD-ab were found, but these only recognized the GAD67 isoform and not the GAD65. Screening of GAD67-ab should be considered in late-onset cerebellar ataxia when GAD65-ab are absent.
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