遗传性克雅氏病。

Nihon rinsho. Japanese journal of clinical medicine Pub Date : 2020-02-10 DOI:10.32388/1c8w9w

H. Toda, H. Kishida, Y. Kuroiwa

{"title":"遗传性克雅氏病。","authors":"H. Toda, H. Kishida, Y. Kuroiwa","doi":"10.32388/1c8w9w","DOIUrl":null,"url":null,"abstract":"Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease (see this term) characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.","PeriodicalId":19307,"journal":{"name":"Nihon rinsho. Japanese journal of clinical medicine","volume":"11 1","pages":"261-5"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Inherited Creutzfeldt-Jakob disease].\",\"authors\":\"H. Toda, H. Kishida, Y. Kuroiwa\",\"doi\":\"10.32388/1c8w9w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease (see this term) characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.\",\"PeriodicalId\":19307,\"journal\":{\"name\":\"Nihon rinsho. Japanese journal of clinical medicine\",\"volume\":\"11 1\",\"pages\":\"261-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nihon rinsho. Japanese journal of clinical medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/1c8w9w\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon rinsho. Japanese journal of clinical medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/1c8w9w","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

遗传性或家族性克雅氏病(fCJD)是一种非常罕见的遗传性朊病毒疾病(见此术语)，以典型的克雅氏病特征(快速进行性痴呆、人格/行为改变、精神障碍、肌颤和共济失调)为特征，具有遗传原因，有时有痴呆家族史。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

[Inherited Creutzfeldt-Jakob disease].

Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease (see this term) characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助