Background: Autoantibodies directed against glutamic acid decarboxylase (GAD-Ab) have recently been described in a few patients with progressive cerebellar ataxia, suggesting an autoimmune physiopathologic mechanism. Objective: To determine the exact role of GAD-Ab and gamma-aminobutyric acid (GABA)-ergic neurotransmission in the pathogenesis of cerebellar ataxia. Design: Case report. Setting: University neurological hospital Patient: We report the case of a patient with subacute cerebellar ataxia associated with GAD-Ab showing periodic alternating nystagmus (PAN). Intervention: Baclofen, a GABAergic medication, was given to the patient. Main Outcome Measures: Eye movement recording of spontaneous nystagmus and postrotatory vestibular responses. Results: Baclofen was effective in suppressing PAN and improving postrotatory vestibular responses but not for improving cerebellar ataxia. Conclusion: The presence of PAN and the response to baclofen provide a unique opportunity to suggest a direct role of GAD-Ab in cerebellar dysfunction in this patient.
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Curtin Univ, Kent St, Perth, WA, Australia
Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, AustraliaCurtin Univ, Kent St, Perth, WA, Australia
Seneviratne, Sinali O.
Buzzard, Katherine A.
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Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia
Monash Univ, Fac Med Nursing & Hlth Sci, Eastern Hlth Clin Sch, Box Hill Hosp, Box Hill, Melbourne, Vic, AustraliaCurtin Univ, Kent St, Perth, WA, Australia
Buzzard, Katherine A.
Cruse, Belinda
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Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, AustraliaCurtin Univ, Kent St, Perth, WA, Australia
Cruse, Belinda
Monif, Mastura
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Royal Melbourne Hosp, Dept Neurol, Melbourne, Vic, Australia
Alfred Hlth, Dept Neurol, Melbourne, Vic, Australia
Univ Melbourne, Dept Physiol, Melbourne, Vic, Australia
Monash Univ, Dept Neurosci, Melbourne, Vic, AustraliaCurtin Univ, Kent St, Perth, WA, Australia