Background: Creutzfeldt-Jakob disease (CJD) is a prion affection that typically produces a rapidly progressive dementia with different neurologic and extra-neurologic manifestations.
Aim: To characterize clinical, imaging and electroencephalography findings in patients with a probable CJD.
Patients And Methods: A case series study of patients admitted in the Neurology department at a public hospital, between 2014 and 2019.