Epilepsy should be suspected in patients with Stiff-person syndrome and new onset paroxysmal episodes. Musicogenic epilepsy may be a manifestation of anti-GAD-Ab spectrum, supporting an autoimmune workup in these patients. Appropriate treatment is not well established, and immunotherapy should be considered in patients with only partial response to antiepileptic drugs.
Keywords: Stiff‐person syndrome; anti‐glutamic acid decarboxylase antibodies; autoimmune epilepsy; musicogenic seizure; reflex seizure; temporal lobe epilepsy.
© 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.