Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, and fatal neurodegenerative disorder. It is caused by **prions**, which are abnormally folded proteins that induce normal proteins in the brain to misfold. CJD primarily affects older adults (sporadic form) worldwide, leading to rapid mental and physical deterioration. Track Creutzfeldt-Jakob disease activity and outbreaks specific to Tennessee.
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Creutzfeldt-Jakob disease was first described in the early 1920s by German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob. Its significance grew with the understanding of transmissible spongiform encephalopathies (TSEs), particularly the link between **variant CJD** and bovine spongiform encephalopathy (BSE) in the 1990s, highlighting the unique nature of prion diseases.
CJD is not contagious through casual contact. Most cases are **sporadic**, meaning they occur spontaneously without a clear cause. Transmission can also occur through medical procedures (**iatrogenic CJD**) involving contaminated brain tissue or instruments, or through inheritance (**familial CJD**); **variant CJD (vCJD)** is acquired by consuming contaminated beef products.
Contagious Period: Varies by disease
Local health department information and state-specific prevention guidance
Our AI-powered surveillance continuously monitors Creutzfeldt-Jakob disease activity across Tennessee. We track data from state health departments, local hospitals, CDC reports, and 50+ global health sources to provide early warning of emerging threats.
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For official state health alerts, vaccination locations, and public health guidance specific to Tennessee, visit your state health department's website.
Whether you live in Tennessee, are traveling there, or have family in the state, understanding Creutzfeldt-Jakob disease prevention is essential. Follow these evidence-based prevention measures:
If you experience symptoms of Creutzfeldt-Jakob disease in Tennessee, contact your healthcare provider immediately. Early diagnosis and treatment improve outcomes significantly.
Emergency symptoms: If you experience severe symptoms, difficulty breathing, or signs of dehydration, call 911 or go to your nearest emergency room.
Trusted information from leading health organizations
Official guidance from the U.S. Centers for Disease Control and Prevention
View CDC Resources βGlobal disease surveillance and guidelines from the World Health Organization
View WHO Resources βDisease information on Virus Watcher is reviewed by our Chief Epidemiologist, a former CDC lead analyst for FluSight forecasting. Outbreak data is aggregated from verified sources including BEACON, ProMED, WHO, CDC, and 50+ national health agencies. This information is for educational purposes and should not replace professional medical advice.
Last reviewed: 2026-06-03
No confirmed cases reported in Tennessee yet. Here are the latest Creutzfeldt-Jakob disease reports from our global surveillance network.
Variant Creutzfeldt-Jakob disease (vCJD) is a fatal prion disorder linked to dietary exposure to bovine spongiform encephalopathy (BSE). The epidemic peaked in the early 2000s, and no new cases have been reported in the UK since 2016. However, uncertainties remain regarding potenβ¦
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