Who is at risk for prion diseases?

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Risk factors for prion disease include:
  • Family history of prion disease
  • Eating meat infected by “mad cow disease”
  • Infection from receiving contaminated corneas or from contaminated medical equipment
How are prion diseases diagnosed?
Prion diseases are confirmed by taking a sample of brain tissue during a biopsy or after death. Healthcare providers, however, can do a number of tests before to help diagnose prion diseases such as CJD, or to rule out other diseases with similar symptoms. Prion diseases should be considered in all people with rapidly progressive dementia.

The tests include:
  • MRI (magnetic resonance imaging) scans of the brain
  • Samples of fluid from the spinal cord (spinal tap, also called lumbar puncture)
  • Electroencephalogram, which analyzes brain waves; this painless test requires placing electrodes on the scalp
  • Blood tests
  • Neurologic and visual exams to check for nerve damage and vision loss
#Alzheimers2018 is coming up with a session on Prion Disease. #Register early to present your work at the #event. To know more download our brochure via: https://bit.ly/2Ld1keT 


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