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: Guidelines for Testing and Treating Long COVID

Join us for an engaging PHO Rounds featuring Dr. Kieran Quinn and Dr. Emilia Liana Falcone, co-chairs of the guideline teams covering the “Pharmacological and Non-Pharmacological Clinical Interventions” and “Testing, Identification and Diagnosis” recommendations for PCC.

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Contact the Department

Communicable Diseases

cd@oahpp.ca

Updated 13 Dec 2024