9 Answers | 4 Thanks
This answers depends on which form of Creutzfeldt-Jakob disease the question is referring to.
Sporadic CJD - It is believed to be the result of a spontaneous conformational change in the native prion protein that occurs…
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Creutzfeldt-Jakob disease (CJD) is a rare and fatal degenerative disease in humans. CJD is one of a group of diseases known as transmissible spongiform encephalopathies (TSE's) or prion disease that affects humans and animals.
CJD affects…
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As Creutzfeldt-Jakob disease (CJD) is transmissible then the answer has to be yes for some forms of CJD but for sporadic CJD, where there is no known cause, then it is unlikely that it can…
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Symptoms that develop and progression of the disease will vary from patient to patient but usually will include
:• Balance and coordination problems
• Headaches
• Challenging behaviour and sometimes aggression
• Visual disturbance
• Incontinence
• Inability to communicate
• Cortical…
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A diagnosis of Creuztzfeldt-Jakob disease (CJD) can only be confirmed by a brain biopsy (not recommended due to transmission risks) or autopsy. In some patients an EEG, MRI and a lumbar puncuture test looking for…
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