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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Medical Sciences
1991
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049699/ https://www.ncbi.nlm.nih.gov/pubmed/1777133 |
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author | Cha, J. K. Kim, M. H. Oh, S. J. Hong, E. K. |
author_facet | Cha, J. K. Kim, M. H. Oh, S. J. Hong, E. K. |
author_sort | Cha, J. K. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-3049699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-30496992011-03-09 A case of Creutzfeldt-Jakob disease. Cha, J. K. Kim, M. H. Oh, S. J. Hong, E. K. J Korean Med Sci Research Article 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. Korean Academy of Medical Sciences 1991-09 /pmc/articles/PMC3049699/ /pubmed/1777133 Text en |
spellingShingle | Research Article Cha, J. K. Kim, M. H. Oh, S. J. Hong, E. K. A case of Creutzfeldt-Jakob disease. |
title | A case of Creutzfeldt-Jakob disease. |
title_full | A case of Creutzfeldt-Jakob disease. |
title_fullStr | A case of Creutzfeldt-Jakob disease. |
title_full_unstemmed | A case of Creutzfeldt-Jakob disease. |
title_short | A case of Creutzfeldt-Jakob disease. |
title_sort | case of creutzfeldt-jakob disease. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049699/ https://www.ncbi.nlm.nih.gov/pubmed/1777133 |
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