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CJD
A guide for patients and carers
How does the brain of someone with CJD differ from normal?
As mentioned above, some people with CJD have deposits or plaques of abnormal bundles of prion protein in their brains, which can be seen on examination after death.This is the most characteristic change and a definitive diagnosis is made based on finding these plaques.Typically, the brain also develops tiny holes where cells have been lost.This makes it look "spongy", hence the name spongiform encephalopathy.
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Contents
- Introduction
- What is CJD?
- What are the different types of CJD?
- What precautions do I need to take to stop CJD spreading?
- Can I get CJD from eating meat?
- How does the brain of someone with CJD differ from normal?
- What causes CJD?
- What does "genetic susceptibility" to CJD mean?
- Is there a genetic test for CJD?
- Can CJD be avoided, and is it catching?
- What are the symptoms of CJD, and how does the disease progress?
- How is CJD diagnosed?
- Are other conditions easily mistaken for CJD?
- How is CJD treated?
- What impact can CJD have on families of poepl with the condition?
- What support is available for carers of people with CJD?
- Conclusion
- Organisations that may be able to help
