Hyperammonemia presenting as opsoclonus–myoclonus–ataxia–tremor syndrome: A case report

Q3 Medicine Annals of Movement Disorders Pub Date : 2022-09-01 DOI:10.4103/aomd.aomd_6_22
S. Manorenj, G. Verma
{"title":"Hyperammonemia presenting as opsoclonus–myoclonus–ataxia–tremor syndrome: A case report","authors":"S. Manorenj, G. Verma","doi":"10.4103/aomd.aomd_6_22","DOIUrl":null,"url":null,"abstract":"Opsoclonus myoclonus syndrome (OMS) is a rare autoimmune condition occurring due to Purkinje cell degeneration due to remote aetiology. Most often it occurs as a paraneoplastic syndrome. Here we report a case of opsoclonus-myoclonus–ataxia tremor syndrome in a 60-year-old woman that occurred due to hyperammonemia and she recovered completely with immunotherapy and correction of hyperammonemia. OMS is the first in literature associated with hyperammonemia.","PeriodicalId":7973,"journal":{"name":"Annals of Movement Disorders","volume":"5 1","pages":"198 - 201"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Movement Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/aomd.aomd_6_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Opsoclonus myoclonus syndrome (OMS) is a rare autoimmune condition occurring due to Purkinje cell degeneration due to remote aetiology. Most often it occurs as a paraneoplastic syndrome. Here we report a case of opsoclonus-myoclonus–ataxia tremor syndrome in a 60-year-old woman that occurred due to hyperammonemia and she recovered completely with immunotherapy and correction of hyperammonemia. OMS is the first in literature associated with hyperammonemia.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
高氨血症表现为视锁肌-肌阵挛-共济失调-震颤综合征:一例报告
肌阵挛综合征(OMS)是一种罕见的自身免疫性疾病,由病因遥远的浦肯野细胞变性引起。最常见的是作为副肿瘤综合征出现。在这里,我们报告了一例60岁女性的视锁肌痉挛-共济失调震颤综合征,该综合征发生于高氨血症,通过免疫治疗和高氨血症矫正,她完全康复。OMS是第一个与高氨血症相关的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Annals of Movement Disorders
Annals of Movement Disorders Medicine-Surgery
CiteScore
0.60
自引率
0.00%
发文量
0
审稿时长
17 weeks
期刊最新文献
Subacute sclerosing panencephalitis presenting as repeated extension of the neck: A case report Mitochondrial membrane protein-associated neurodegeneration presenting with pure motor neuropathy: A rare case report and review of the literature SCA 15 presenting with parkinsonism–dystonia, tremor, and psychosis in an Indian woman The impact of bilateral subthalamic nucleus deep brain stimulation on dyskinesia and levodopa equivalent daily dose in advanced Parkinson’s disease An interesting case of ocular flutter, myoclonus, and ataxia in the postpartum period
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1