| Literature DB >> 27806870 |
Mar Guasp1, Nuria Solà-Valls1, Eugenia Martínez-Hernández2, M Pilar Gil3, Cristina González3, Luis Brieva3, Albert Saiz4, Josep Dalmau5, Francesc Graus4, Helena Ariño6.
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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27806870 PMCID: PMC5831398 DOI: 10.1016/j.jneuroim.2016.09.019
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478