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 Microbiology Rounds: Implementation of Enteric Protozoa PCR at PHO

This session will outline the routine indications for testing of these protozoans, explain the methodologies that will be used and summarize the new algorithmic criteria for testing.

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Contact the Department

Communicable Diseases

cd@oahpp.ca

Updated 13 Dec 2024