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kuru

File:Fore_child_in_advanced_kuru_stage.png · Wikimedia Commons · See Wikimedia Commons

EntityQ274615· pop 52· linked from 98 articles

Also known as kuru encephalopathy

Doença neurodegenerativa rara causada por príons

AI overview

I appreciate your request, but the context you've provided ("human disease") is too general for me to write an accurate overview of kuru specifically. To be reliable and accurate, I would need more detailed source information about kuru's specific characteristics, history, or significance. I don't want to risk including inaccurate details by relying only on this minimal context.

AI-generated from the Wikipedia summary — may contain errors.

Key facts

Pronunciation
/ˈkʊ.ɹuː/
Specialty
Neuropathology , infectious disease
Symptoms
Body tremors, random outbursts of laughter, emotional degradation, gradual loss of coordination
Complications
Infection and pneumonia during the terminal stage.
Usual onset
5 to 50 years after initial exposure
Duration
11 to 14 months life expectancy after onset of symptoms
Causes
Transmission of infectious prion proteins
Risk factors
Cannibalism , especially consumption of human brains
Diagnostic method
Autopsy
Differential diagnosis
Creutzfeldt–Jakob disease
Prevention
Not eating infected humans
Treatment
Supportive care
Prognosis
Always fatal
Frequency
Extinct (last case in 2009)
Deaths
Approximately 2,700

via Wikipedia infobox

Research

2,047 papers

via PubMed

Wikidata facts

Subclass of
disease
Image
Fore child in advanced kuru stage.png
Show 10 more facts
different from
Kuru Kingdom
Commons category
Kuru (disease)
health specialty
neurology
ICD-9-CM
046.0
on focus list of Wikimedia project
WikiProject Medicine
has cause
prion
medical examination
histopathology
symptoms and signs
dementia
possible treatment
symptomatic treatment
Sources (5)

via Wikidata · CC0

Article · Português

Kuru é o nome local da Doença de Creutzfeldt-Jakob clássica. Ocorreu como que uma epidemia (apesar de já ter sido declarado pelo Guinness Book como doença mais rara da Terra) nas décadas de 1950 e 1960 entre os papuas, um grupo de pessoas nativas da Nova Guiné. Descobriu-se que a causa próxima era a prática da antropofagia. Apresentando os sintomas da DCJ, essa doença vitimava principalmente mulheres e crianças, as pessoas que ingeriam cerimonialmente o cérebro de seus familiares mortos, em um ritual de luto. A antropofagia foi apontada como o mecanismo de transmissão de príons na doença, que ficou conhecida como Kuru. A descoberta desta doença infecciosa rendeu ao pesquisador D. Carleton Gajdusek o Nobel de Fisiologia ou Medicina, no ano de 1976.

Abstract from DBpedia / Wikipedia · CC BY-SA

Gallery (3)