J Korean Med Sci.  1991 Sep;6(3):273-278. 10.3346/jkms.1991.6.3.273.

A case of Creutzfeldt-Jakob disease

Affiliations
  • 1Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea.

Abstract

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 to a vegetative state, becomes comatous, and is ultimately dead within several months. The authors present a case of Creutzfeldt-Jakob disease, proved by clinical findings, typical serial EEG, and pathologic features.

Keyword

Creutzfeldt-Jakob disease

MeSH Terms

Creutzfeldt-Jakob Syndrome/*diagnosis/pathology/radiography
Electroencephalography
Female
Humans
Middle Aged
Tomography, X-Ray Computed
Full Text Links
  • JKMS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr