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The disease is an extremely rare brain disorder that causes dementia.
Creutzfeldt-Jakob disease (CJD), also known as subacute spongiform encephalopathy or prion disease neurocognitive disorder, is a fatal degenerative brain disorder. Memory problems, behavioral changes, poor coordination, and visual disturbances are among the early symptoms. Dementia, involuntary movements, blindness, weakness, and coma are later symptoms. Approximately 70% of people die within a year of being diagnosed. Walther Spielmeyer coined the term Creutzfeldt-Jakob disease in 1922, after the German neurologists Hans Gerhard Creutzfeldt and Alfons Maria Jakob.
Creutzfeldt-Jakob disease (CJD) is caused by a prion, which is an abnormal infectious protein in the brain. Proteins are amino acid-based molecules that help our bodies' cells function. They begin as a string of amino acids that fold into a three-dimensional shape. They may experience discomfort, and some of the disease's symptoms, such as myoclonus, can be distressing to caregivers. Neurologists believe that the disease itself causes no pain.
To learn more about Creutzfeldt-Jakob disease, here
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