Creutzfeldt-Jakob Disease (cont.)
In this Article
- What is Creutzfeldt-Jakob disease (CJD)?
- What are the symptoms of the Creutzfeldt-Jakob disease?
- How is Creutzfeldt-Jakob disease diagnosed?
- What causes Creutzfeldt-Jakob disease?
- How is Creutzfeldt-Jakob disease transmitted?
- What research is taking place with Creutzfeldt-Jakob disease?
- How can I help research?
- Where can I get more information about Creutzfeldt-Jakob disease?
- How is the Creutzfeldt-Jakob disease treated?
What are the Symptoms of the Disease?
CJD is characterized by rapidly progressive dementia. Initially, individuals experience problems with muscular coordination; personality changes, including impaired memory, judgment, and thinking; and impaired vision. People with the disease also may experience insomnia, depression, or unusual sensations. CJD does not cause a fever or other flu-like symptoms. As the illness progresses, mental impairment becomes severe. Individuals often develop involuntary muscle jerks called myoclonus, and they may go blind. They eventually lose the ability to move and speak and enter a coma. Pneumonia and other infections often occur in these individuals and can lead to death.
There are several known variants of CJD. These variants differ somewhat in the symptoms and course of the disease. For example, a variant form of the disease-called new variant or variant (nv-CJD, v-CJD), described in Great Britain and France-begins primarily with psychiatric symptoms, affects younger individuals than other types of CJD, and has a longer than usual duration from onset of symptoms to death. Another variant, called the panencephalopathic form, occurs primarily in Japan and has a relatively long course, with symptoms often progressing for several years. Scientists are trying to learn what causes these variations in the symptoms and course of the disease.
Some symptoms of CJD can be similar to symptoms of other progressive neurological disorders, such as Alzheimer's or Huntington's disease. However, CJD causes unique changes in brain tissue which can be seen at autopsy. It also tends to cause more rapid deterioration of a person's abilities than Alzheimer's disease or most other types of dementia.
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