Creutzfeldt-Jakob Disease (CJD)

Creutzfeldt-Jakob Disease (CJD) is a fatal neurodegenerative disorder caused by the development of abnormal, infective proteins called prions. It is rare in Ontario. CJD can occur sporadically, due to inherited genetic mutations or through exposure to an incorrectly reprocessed medical instrument used on an infective patient. Variant CJD is related to consumption of infected beef.

Event

PHO Rounds: Toxigenic C. Diphtheriae in a Donkey: Implications for Zoonotic Disease Transmission and One Health Approach

Enhanced disease surveillance, along with clearer protocols for reporting and information sharing across sectors, is essential to reduce the risk of future zoonotic outbreaks and protect public health.

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