Cargando…
Creutzfeldt-Jakob disease: recent developments
Creutzfeldt-Jakob disease (CJD) is a rare prion disorder that has been the subject of both professional and public interest following the identification of variant CJD as a zoonotic disorder. There have been recent advances in diagnostic techniques, including real-time quaking-induced conversion and...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710312/ https://www.ncbi.nlm.nih.gov/pubmed/29225787 http://dx.doi.org/10.12688/f1000research.12681.1 |
_version_ | 1783282929331339264 |
---|---|
author | Mackenzie, Graeme Will, Robert |
author_facet | Mackenzie, Graeme Will, Robert |
author_sort | Mackenzie, Graeme |
collection | PubMed |
description | Creutzfeldt-Jakob disease (CJD) is a rare prion disorder that has been the subject of both professional and public interest following the identification of variant CJD as a zoonotic disorder. There have been recent advances in diagnostic techniques, including real-time quaking-induced conversion and magnetic resonance imaging brain scan, that have allowed more accurate case recognition in all forms of CJD. Although the epidemic of variant CJD is clearly in decline, prevalence studies suggest that it may be premature to be complacent about concerns for public health. |
format | Online Article Text |
id | pubmed-5710312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-57103122017-12-07 Creutzfeldt-Jakob disease: recent developments Mackenzie, Graeme Will, Robert F1000Res Review Creutzfeldt-Jakob disease (CJD) is a rare prion disorder that has been the subject of both professional and public interest following the identification of variant CJD as a zoonotic disorder. There have been recent advances in diagnostic techniques, including real-time quaking-induced conversion and magnetic resonance imaging brain scan, that have allowed more accurate case recognition in all forms of CJD. Although the epidemic of variant CJD is clearly in decline, prevalence studies suggest that it may be premature to be complacent about concerns for public health. F1000 Research Limited 2017-11-27 /pmc/articles/PMC5710312/ /pubmed/29225787 http://dx.doi.org/10.12688/f1000research.12681.1 Text en Copyright: © 2017 Mackenzie G and Will R http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Mackenzie, Graeme Will, Robert Creutzfeldt-Jakob disease: recent developments |
title | Creutzfeldt-Jakob disease: recent developments |
title_full | Creutzfeldt-Jakob disease: recent developments |
title_fullStr | Creutzfeldt-Jakob disease: recent developments |
title_full_unstemmed | Creutzfeldt-Jakob disease: recent developments |
title_short | Creutzfeldt-Jakob disease: recent developments |
title_sort | creutzfeldt-jakob disease: recent developments |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710312/ https://www.ncbi.nlm.nih.gov/pubmed/29225787 http://dx.doi.org/10.12688/f1000research.12681.1 |
work_keys_str_mv | AT mackenziegraeme creutzfeldtjakobdiseaserecentdevelopments AT willrobert creutzfeldtjakobdiseaserecentdevelopments |