any of a group of fatal neurodegenerative diseases caused by self-replicating abnormal
prion proteins in the brain. Symptoms include gait disturbance, lack of coordination, muscle tremors and jerks, and difficulty in swallowing. Human varieties include
Creutzfeldt–Jakob disease,
fatal familial insomnia, Gerstmann–Straussler–Scheinker syndrome, and
kuru. Prion diseases are also known as
spongiform encephalopathies because of the postmortem appearance of the brain.