Uca, Ali UlviGenc, Bulent OguzGuney, FigenAkpinar, Zehra2024-02-232024-02-2320141300-7157https://doi.org/10.5505/epilepsi.2014.86158https://hdl.handle.net/20.500.12452/16914Sporadic Creutzfeldt- Jakob disease (sCJD) is the most common disorder among the very rare prion diseases (human transmissible subacute spongiform encephalopathies). The diagnosis might be easy if a patient with characteristics features of myoclonus, progressive dementia and periodic electroencephalography activity. Diagnosis of some patients with unusual symptoms and signs may be challenging. The reported case is a 65 years old female patient who was finally diagnosed as CJD, after previously being misdiagnosed with depression, dementia and refractory nonconvulsive status epilepticus.trinfo:eu-repo/semantics/closedAccessCreutzfeldt-Jakob DiseaseNonconvulsive Status EpilepticusPrion DiseaseArticle2028792WOS:00040885190000710.5505/epilepsi.2014.86158