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Creutzfeldt-Jakob Disease

Creutzfeldt-Jakob disease (CJD) is a rare, degenerative brain disorder. Symptoms usually start around age 60. Memory problems, behavior changes, vision problems, and poor muscle coordination progress quickly to dementia, coma, and death. Most patients die within a year.

The three main categories of CJD are :

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Results 1 - 10 of 61 for "Creutzfeldt-Jakob" Disease
  1. Creutzfeldt-Jakob Disease (National Library of Medicine)  
    Creutzfeldt-Jakob disease (CJD) is a rare, degenerative brain disorder. Symptoms usually start around age 60. Memory problems, behavior ...
  2. Creutzfeldt-Jakob Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Creutzfeldt-Jakob Disease/Start Here ... Creutzfeldt-Jakob Disease ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health
  3. Creutzfeldt-Jakob Disease (Alzheimer's Association)  
    Creutzfeldt-Jakob disease – learn about CJD symptoms, diagnosis, causes and treatments and how this disorder relates to Alzheimer's and ...
  4. Creutzfeldt-Jakob disease (CJD) is a form of brain damage that leads to a rapid decrease in movement and ...
  5. Creutzfeldt-Jakob disease is an organic brain syndrome caused by a protein-like particle called a prion. Loss of ...
  6. Variant Creutzfeldt-Jakob Disease (vCJD) (Centers for Disease Control and Prevention)  
    Variant Creutzfeldt-Jakob Disease (vCJD), Prion Diseases
  7. Variant Creutzfeldt-Jakob Disease (vCJD): Risk for Travelers (Centers for Disease Control and Prevention)  
    Variant Creutzfeldt-Jakob Disease (vCJD)
  8. ... which have overlapping signs and symptoms, include familial Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker syndrome (GSS), and fatal ... PrPSc. Sporadic forms of prion disease include sporadic Creutzfeldt-Jakob disease (sCJD), sporadic fatal insomnia (sFI), and variably protease- ...
  9. ... people with familial forms of prion disease, including Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker syndrome (GSS), and fatal ... GSS MGC26679 PRIO_HUMAN prion protein (p27-30) (Creutzfeldt-Jakob disease, Gerstmann-Strausler-Scheinker syndrome, fatal familial insomnia) PRIP ...
  10. Creutzfeldt-Jakob Disease/Diagnosis and Tests ... Creutzfeldt-Jakob Disease
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