Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3051796 | Epilepsy & Behavior Case Reports | 2014 | 5 Pages |
Abstract
Seizures are known to occur in Creutzfeldt–Jakob disease (CJD). In the setting of a rapidly progressive condition with no effective therapy, determining appropriate treatment for seizures can be difficult if clinical morbidity is not obvious yet the electroencephalogram (EEG) demonstrates a worrisome pattern such as status epilepticus. Herein, we present the case of a 39-year-old man with CJD and electrographic seizures, discuss how this case challenges conventional definitions of seizures, and discuss a rational approach toward treatment. Coincidentally, our case is the first report of CJD in a patient with Stickler syndrome.
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Authors
Marcus C. Ng, M. Brandon Westover, Andrew J. Cole,