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  1. Also known as: CJD, subacute spongiform encephalopathy
    Content medically reviewed by
    Dr. Karthikeya T Mverified specialist
    MD, Internal Medicine
    View full profile onLinkedIn logoLinkedIn
    An unusual neurologic disorder that leads to dementia followed by death. This is very rare condition.
    Condition Highlight
    Urgent medical attention is usually recommended by healthcare providers
    Is condition treatable?
    Treatments can help manage condition, no known cure
    Does diagnosis require lab test or imaging?
    Often requires lab test or imaging
    Time taken for recovery
    Can last several years or be lifelong
    How is condition transmitted?
    Transmitted through direct contact
    Condition Highlight
    Common for ages 60 and older
    Condition Highlight
    Family history may increase likelihood
    Condition Image
    Source: Focus Medica . For informational purposes only. Consult a medical professional for advice. Learn more
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  2. WebMay 8, 2024 · Creutzfeldt-Jakob disease (CJD) belongs to the family of diseases known as transmissible spongiform encephalopathies (TSEs) or prion-related diseases. Prion diseases in humans occur in 3...

  3. Dealing with Creutzfeldt-Jakob Disease - happiesthealth.com

  4. Web2 days ago · A prion disease is a type of proteopathy, or disease of structurally abnormal proteins. In humans, prions are believed to be the …

  5. Understanding Creutzfeldt-Jakob disease in Iran: a systematic …

  6. Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10 …

  7. Understanding Creutzfeldt-Jakob disease in Iran: a systematic …

  8. (PDF) Understanding Creutzfeldt-Jakob disease in Iran: a …

  9. Prion meeting 2023: implications of a growing field - PubMed

  10. Absence of evidence of transfusion transmission risk of Creutzfeldt ...

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