Kuru [kuru]

topical
19
Terms

Encephalopathy, Kuru
Kuru Encephalopathy

Persistent link   https://www.medvik.cz/link/D007729
Definition

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)

Annotation
do not confuse with KORO, a depersonalization disord
DUI
D007729 MeSH Browser
CUI
M0012084

C Diseases
C01 Infections 2 026
C01.207.800 Prion Diseases 175
C01.207.800.230 Creutzfeldt-Jakob Syndrome 246
C01.207.800.392 Insomnia, Fatal Familial 10
C01.207.800.435 Kuru 19
C01.207.800.717 Scrapie 27
C01.207.800.858 Wasting Disease, Chronic 11
C10.228.228.800 Prion Diseases 175
C10.228.228.800.230 Creutzfeldt-Jakob Syndrome 246
C10.228.228.800.392 Insomnia, Fatal Familial 10
C10.228.228.800.435 Kuru 19
C10.228.228.800.717 Scrapie 27
C10.228.228.800.858 Wasting Disease, Chronic 11
C10.574.843 Prion Diseases 175
C10.574.843.512 Insomnia, Fatal Familial 10
C10.574.843.625 Kuru 19
C10.574.843.850 Scrapie 27
C10.574.843.925 Wasting Disease, Chronic 11