进行性核上性麻痹(PSP)伴多系统萎缩1例

R. Judah Rajendran, Kannan Ramesh, Prasanth Hannah Ranjee
{"title":"进行性核上性麻痹(PSP)伴多系统萎缩1例","authors":"R. Judah Rajendran, Kannan Ramesh, Prasanth Hannah Ranjee","doi":"10.29328/journal.ijceo.1001038","DOIUrl":null,"url":null,"abstract":"Multi System Atrophy is a rare neurodegenerative, synucleinopathic disorder which progresses rapidly. It often presents with symptoms similar to Parkinsonism posing a diagnostic dilemma. It is an orphan disease with an annual incidence of 0.1 to 3 per 100,000, with many being revealed only on autopsy, following years of treatment for Parkinson’s disease. There are very few cases reported from India, possibly because diagnosis requires a high index of suspicion, coupled with a comprehensive knowledge of the disease in order to detect it early and prevent progression.","PeriodicalId":359167,"journal":{"name":"International Journal of Clinical and Experimental Ophthalmology","volume":"67 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A case report of Multi System Atrophy (MSA) with cross over features of Progressive Supranuclear Palsy (PSP)\",\"authors\":\"R. Judah Rajendran, Kannan Ramesh, Prasanth Hannah Ranjee\",\"doi\":\"10.29328/journal.ijceo.1001038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Multi System Atrophy is a rare neurodegenerative, synucleinopathic disorder which progresses rapidly. It often presents with symptoms similar to Parkinsonism posing a diagnostic dilemma. It is an orphan disease with an annual incidence of 0.1 to 3 per 100,000, with many being revealed only on autopsy, following years of treatment for Parkinson’s disease. There are very few cases reported from India, possibly because diagnosis requires a high index of suspicion, coupled with a comprehensive knowledge of the disease in order to detect it early and prevent progression.\",\"PeriodicalId\":359167,\"journal\":{\"name\":\"International Journal of Clinical and Experimental Ophthalmology\",\"volume\":\"67 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Clinical and Experimental Ophthalmology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29328/journal.ijceo.1001038\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical and Experimental Ophthalmology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29328/journal.ijceo.1001038","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

摘要多系统萎缩是一种罕见的神经退行性、突触性疾病,其进展迅速。它通常表现出与帕金森症相似的症状,使诊断陷入困境。这是一种孤儿病,年发病率为每10万人0.1至3人,其中许多人只有在对帕金森病进行多年治疗后才在尸检中发现。印度报告的病例很少,可能是因为诊断需要高度的怀疑指数,再加上对疾病的全面了解,以便及早发现并防止进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case report of Multi System Atrophy (MSA) with cross over features of Progressive Supranuclear Palsy (PSP)
Multi System Atrophy is a rare neurodegenerative, synucleinopathic disorder which progresses rapidly. It often presents with symptoms similar to Parkinsonism posing a diagnostic dilemma. It is an orphan disease with an annual incidence of 0.1 to 3 per 100,000, with many being revealed only on autopsy, following years of treatment for Parkinson’s disease. There are very few cases reported from India, possibly because diagnosis requires a high index of suspicion, coupled with a comprehensive knowledge of the disease in order to detect it early and prevent progression.
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
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信