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A case of Creutzfeldt-Jakob disease.

Creutzfeldt-Jakob disease (CJD) is presumably caused by a slow infectious pathogen or prion. The principal clinical features of Creutzfeldt-Jakob disease are dementia, pyramidal and extrapyramidal symptoms and signs, cerebellar dysfunction, and myoclonus. The patient rapidly deteriorates, declines t...

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Bibliographic Details
Main Authors: Cha, J. K., Kim, M. H., Oh, S. J., Hong, E. K.
Format: Artigo
Language:Inglês
Published: Korean Academy of Medical Sciences 1991
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3049699/
https://ncbi.nlm.nih.gov/pubmed/1777133
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