Creutzfeldt–Jakob disease in the Republic of Sakha (Yakutia)
Creutzfeldt–Jakob disease (CJD) is a rare neurodegenerative disease caused by the accumulation of the pathological isoform of prion protein. The classic clinical presentation of CJD is characterized by rapidly progressive dementia, ataxia, myoclonus, and akinetic mutism at the terminal stage of the...
Published in: | Neurology, Neuropsychiatry, Psychosomatics |
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Main Authors: | , , , , , , |
Format: | Article in Journal/Newspaper |
Language: | Russian |
Published: |
IMA-PRESS LLC
2020
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Subjects: | |
Online Access: | https://doi.org/10.14412/2074-2711-2020-2-86-91 https://doaj.org/article/801316aa23d948f58cbc0c19c0cf3cc8 |