{"title":"CJD:病例报告","authors":"Neema Agarwal, S. Agarwal","doi":"10.5580/2c9a","DOIUrl":null,"url":null,"abstract":"Creuzfeldt-Jakob’s Disease (CJD) is a rare neurodegenerative disorder that is included among the transmissible spongiform encephalopathies. The clinical features are those of a rapidly progressive dementia with myoclonic jerks culminating in death in less than one year. We intend to highlight the role of the magnetic resonance imaging (MRI) as a vital tool for the presumptive in vivo diagnosis, thereby obviating the need of histopathologic confirmation of the disease.","PeriodicalId":22526,"journal":{"name":"The Internet Journal of Radiology","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2012-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CJD: A Case Report\",\"authors\":\"Neema Agarwal, S. Agarwal\",\"doi\":\"10.5580/2c9a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Creuzfeldt-Jakob’s Disease (CJD) is a rare neurodegenerative disorder that is included among the transmissible spongiform encephalopathies. The clinical features are those of a rapidly progressive dementia with myoclonic jerks culminating in death in less than one year. We intend to highlight the role of the magnetic resonance imaging (MRI) as a vital tool for the presumptive in vivo diagnosis, thereby obviating the need of histopathologic confirmation of the disease.\",\"PeriodicalId\":22526,\"journal\":{\"name\":\"The Internet Journal of Radiology\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Internet Journal of Radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5580/2c9a\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet Journal of Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/2c9a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Creuzfeldt-Jakob’s Disease (CJD) is a rare neurodegenerative disorder that is included among the transmissible spongiform encephalopathies. The clinical features are those of a rapidly progressive dementia with myoclonic jerks culminating in death in less than one year. We intend to highlight the role of the magnetic resonance imaging (MRI) as a vital tool for the presumptive in vivo diagnosis, thereby obviating the need of histopathologic confirmation of the disease.
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