U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Kuru

A prion disease found exclusively among the Fore linguistic group natives of the highlands of NEW GUINEA. The illness is primarily restricted to adult females and children of both sexes. It is marked by the subacute onset of tremor and ataxia followed by motor weakness and incontinence. Death occurs within 3-6 months of disease onset. The condition is associated with ritual cannibalism, and has become rare since this practice has been discontinued. Pathologic features include a noninflammatory loss of neurons that is most prominent in the cerebellum, glial proliferation, and amyloid plaques. (From Adams et al., Principles of Neurology, 6th ed, p773)

PubMed search builder options

Subheadings:

Tree Number(s): C01.207.800.435, C10.228.228.800.435, C10.574.843.625

MeSH Unique ID: D007729

Entry Terms:

  • Kuru Encephalopathy
  • Encephalopathy, Kuru

Supplemental Content

Loading ...