Variant Creutzfeldt-Jakob disease (vCJD) is a type of prion disease that can cause death. Bovine spongiform encephalopathy (BSE) is a prion disease in cows. There is evidence that BSE can spread to humans. This results in vCJD. It is also known as mad cow disease.
It is believed that vCJD is caused by proteins called prions. Prions are normal proteins in the body. These prions may fold up in a way that is not normal. This can change them into the protein that causes the illness. The buildup of these prions may be linked to vCJD.
The Nervous System
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Variant CJD is more common in younger people. Being around tissue that contains prions may raise the risk. This may happen from:
After a person is exposed, it can take up to 20 years until they feel sick. Problems get worse over time and include:
The doctor will ask about your symptoms and health history. A physical exam will be done.
These tests may be done to learn more about the brain:
Images may be taken with:
The only way to diagnose vCJD is for a doctor to look at the brain after a person has died.
There is no cure for vCJD. You will receive support and help easing discomfort.
The risk of this problem may be lowered by not eating beef products when traveling to places where BSE is a problem.
Creutzfeldt-Jakob Disease Foundation, Inc.
National Institute of Neurological Disorders and Stroke
Public Health Agency of Canada
Creutzfeldt-Jakob disease. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/creutzfeldt-jakob-disease. Accessed January 25, 2021.
Creutzfeldt-Jakob disease fact sheet. National Institute of Neurological Disorders and Stroke website. Available at:
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Accessed January 25, 2021.
Geschwind MD. Prion Diseases. Continuum (Minneap Minn). 2015 Dec;21(6 Neuroinfectious Disease):1612-1638.
Mackenzie G, Will R. Creutzfeldt-Jakob disease: recent developments. F1000res. 2017;6:2053.
Last reviewed December 2020 by
EBSCO Medical Review Board
Rimas Lukas, MD
Last Updated: 1/25/2021