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A progressive, fatal form of spongiform encephalopathy endemic to Fore people in the highlands of New Guinea, initially attributed to a “slow virus” infection, but now known to be caused by prions. Transmission is believed to be effected by contamination and ingestion during ritual cannabalism. It is characterized by ataxia, tremors, lack of coordination and death; pathological lesions in the brain include neuronal loss, ostrocytosis and status spongiosus. See prion. [native dialect, to shiver from fear or cold]
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ku·ru 'ku̇(ə)r-(.)ü n a rare progressive fatal spongiform encephalopathy that is caused by a prion, resembles Creutzfeldt-Jakob disease, and has occurred among tribespeople in eastern New Guinea who engaged in a form of ritual cannibalism called also laughing death, laughing sickness
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n.
a disease that affects only members of the Fore tribe of New Guinea. It involves a progressive degeneration of the nerve cells of the central nervous system, particularly in the region of the brain that controls movement. Muscular control becomes defective and shiver-like tremors occur in the trunk, limbs, and head. Kuru affects mainly women and children and usually proves fatal within 9-12 months. It is thought to be caused by a prion and transmitted by cannibalism. See also spongiform encephalopathy.
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ku·ru (kooґroo) [“shivering†in language of the Fore people of New Guinea] an infectious form of prion disease with a long incubation period, found only among the Fore and neighboring peoples of New Guinea and thought to be associated with ritual cannibalism. It is manifested by truncal and limb ataxia, a shivering-like tremor, and dysarthria and ends invariably in death; strabismus and extrapyramidal symptoms may also be found. Amyloid plaques are present in about two thirds of affected individuals.Medical dictionary. 2011.