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It belongs to a group of human and animal diseases known as prion disorders It is caused by prions, infectious, misshapen versions of normal proteins, which build up in the brain, damaging brain cells. [4][1] early symptoms include memory problems, behavioral changes, poor coordination, visual disturbances and auditory disturbances

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Infection usually leads to death within one year of symptom onset. The incidence of cjd cases worldwide is one to two cases, per million individuals, per year. <1% of cases are iatrogenic or variant cjd.

It’s usually fatal within a year.

Prions are normal proteins that have changed their shape Healthy proteins have a healthy shape, which allows them to function normally. In the united states there are nearly 500 new cjd cases per year