The role of IL-1β in Regulating Seizure Susceptibility in Creutzfeldt-Jakob Disease
Tam Thanh Nguyen Tran Introduction: Creutzfeldt-Jakob Disease is a rare (1-1.5 cases per million worldwide), rapidly progressive, and inevitably fatal neurodegenerative prion disease involving abnormal protein aggregates that cause brain tissue deterioration (1,2). The normal prion protein PrPC (cellular) is mutated to the infectious form PrPSc (prototypical prion disease–scrapie) that…