Kuru with incubation periods exceeding two decades
Abstract
The clinical characteristics of kuru in 15 patients are described. All the patients had a history of joint pains preceding difficulty walking. The severity of the neurological dysfunction varied from mild truncal and limb ataxia necessitating the use of a stick for walking to terminal illness accompanied by marked ataxia, rigidity, spasticity, and dementia. All the patients with kuru in this study had a apprehensive, frightened facial expression. Most of the patients examined showed diminished or absent optokinetic nystagmus bilaterally. Apprehensive facies and diminished optokinetic nystagmus have not previously been described in kuru. The other clinical features of the current patients with kuru are similar to those recorded twenty years ago. Epidemiological surveillance, anamnesis, and missionary reports strongly suggest that all the patients described in this study were exposed to the kuru agent more than two decades ago through ritualistic cannibalism. Thus the incubation period or time interval from exposure to the onset of clinical illness exceeds two decades, while the duration of illness is two years or less. The cause of these extraordinarily long incubation periods is unknown but may result in part from exposure to small doses of the kuru agent through an inefficient oral route.
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Kuru is a uniformly fatal and remarkably stereotyped cerebellar ataxic syndrome accompanied by tremor and choreiform and athetoid movements.
“Kuru is a uniformly fatal and remarkably stereotyped cerebellar ataxic syndrome accompanied by tremor and choreiform and athetoid movements (27, 39, 57–61)”
From Kuru (2012) · cites this paper as [61]
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Kuru, the First Human Prion Disease
Liberski, P. P., Gajos, A., Sikorska, B., & Lindenbaum, S. (2019) · Viruses · doi:10.3390/v11030232 · Cited by 69 · see citing works
Liberski, P. P., Sikorska, B., Lindenbaum, S., Goldfarb, L. G., McLean, C., Hainfellner, J. A., & Brown, P. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3182444efd · Cited by 50 · see citing works
- Authors
- Prusiner, S. B., Gajdusek, D. C., & Alpers, M. P.
- Affiliations
- University of California, San Francisco (US)
- National Institutes of Health (US)
- Papua New Guinea Institute of Medical Research (PG)
- Corresponding author
- Prusiner, Stanley B.
- ORCID
- Prusiner, Stanley B.
- Venue
- Annals of Neurology
- Publisher
- Wiley
- Published
- 1982-07
- Volume
- 12
- Issue
- 1
- Pages
- 1-9
- ISSN
- 0364-5134 (ISSN-L)
- 1531-8249
- OpenAlex
- W2037682293
- Cited by
- 63
- References
- 0
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 2 · 2021: 1 · 2019: 1 · 2017: 2 · 2014: 1 · 2013: 2 · 2012: 1
- FWCI
- 1.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Prion Diseases and Protein Misfolding
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Amyloidosis: Diagnosis, Treatment, Outcomes
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
- Keywords
- kuru, long incubation period, prion disease, ataxia, optokinetic nystagmus, facial expressions, clinical features
- MeSH terms
- Adult, Cannibalism, Ceremonial Behavior, Female, Humans, Kuru, Male, Middle Aged, New Guinea, Reflex, Abnormal
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