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- W4234580599 abstract "<strong>Background:</strong> The clinical spectrum of anti-glutamic acid decarboxylase (GAD) antibody-associated neurologic syndromes is expanding, with focal, generalized, and atypical forms. <strong>Case Report:</strong> We describe a 59-year-old female showing continuous right lower limb myoclonus and mild encephalopathy. These symptoms started 2 weeks prior to evaluation. The patient had great improvement with intravenous steroids. An autoantibody panel was positive for anti-GAD. <strong>Discussion:</strong> Various clinical manifestations, including myoclonus, may relate to anti-GAD antibodies. The treatment options available include symptomatic drugs, intravenous immunoglobulin, steroids, and other immunosuppressant agents." @default.
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- W4234580599 date "2018-11-01" @default.
- W4234580599 modified "2023-10-18" @default.
- W4234580599 title "Anti-GAD Antibody-associated Syndrome Presenting with Limb Myoclonus" @default.
- W4234580599 doi "https://doi.org/10.5334/tohm.421" @default.
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