[Neurophysiological (evoked auditory and somatosensory potentials) and neuroradiological (cranial CT) study in patients with olivopontocerebellar atrophy].

L Rossi, F Zappoli, G De Scisciolo, P Marini, G Russo, A Bindi
{"title":"[Neurophysiological (evoked auditory and somatosensory potentials) and neuroradiological (cranial CT) study in patients with olivopontocerebellar atrophy].","authors":"L Rossi,&nbsp;F Zappoli,&nbsp;G De Scisciolo,&nbsp;P Marini,&nbsp;G Russo,&nbsp;A Bindi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Thirteen patients affected by either dominant or recessive and/or sporadic olivopontocerebellar atrophy were studied. All patients were subjected to auditory evoked potential recordings including early and long latency components, CT scans, vestibular and EMG-ENG examinations. In nine patients somatosensory evoked potentials were also recorded. Clear-cut abnormalities in brainstem auditory evoked potentials were observed in only two patients while a slight reduction of the IV-V/I amplitude ratio was found in seven cases. N85 was increased in two patients. The main feature of somatosensory evoked potentials abnormalities was a delayed N20 in association with prolonged N13-N20 central conduction time (five patients). For all patients the CT scan varying degrees of cerebellar and brainstem atrophy. There was no clear correlation between the abnormalities revealed by neurophysiological and neuroradiological investigations and the severity and duration of the illness. It is noteworthy that auditory and/or somatosensory evoked potential changes were found in all dominant olivopontocerebellar atrophy patients.</p>","PeriodicalId":21409,"journal":{"name":"Rivista di patologia nervosa e mentale","volume":"105 4","pages":"187-99"},"PeriodicalIF":0.0000,"publicationDate":"1984-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rivista di patologia nervosa e mentale","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Thirteen patients affected by either dominant or recessive and/or sporadic olivopontocerebellar atrophy were studied. All patients were subjected to auditory evoked potential recordings including early and long latency components, CT scans, vestibular and EMG-ENG examinations. In nine patients somatosensory evoked potentials were also recorded. Clear-cut abnormalities in brainstem auditory evoked potentials were observed in only two patients while a slight reduction of the IV-V/I amplitude ratio was found in seven cases. N85 was increased in two patients. The main feature of somatosensory evoked potentials abnormalities was a delayed N20 in association with prolonged N13-N20 central conduction time (five patients). For all patients the CT scan varying degrees of cerebellar and brainstem atrophy. There was no clear correlation between the abnormalities revealed by neurophysiological and neuroradiological investigations and the severity and duration of the illness. It is noteworthy that auditory and/or somatosensory evoked potential changes were found in all dominant olivopontocerebellar atrophy patients.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[脑桥小脑萎缩患者的神经生理学(诱发听觉和体感电位)和神经影像学(颅脑CT)研究]。
本文对13例显性或隐性和/或散发性橄榄桥小脑萎缩患者进行了研究。所有患者均接受听觉诱发电位记录,包括早期和长潜伏期成分、CT扫描、前庭和肌电图检查。同时记录了9例患者的体感诱发电位。仅2例患者脑干听觉诱发电位明显异常,7例患者脑干听觉诱发电位振幅比轻微降低。2例患者N85升高。体感诱发电位异常的主要特征是N20延迟,与N13-N20中枢传导时间延长有关(5例)。所有患者的CT扫描均显示不同程度的小脑和脑干萎缩。神经生理学和神经放射学检查显示的异常与疾病的严重程度和持续时间之间没有明确的相关性。值得注意的是,听觉和/或体感觉诱发电位的变化发现在所有优势橄榄桥小脑萎缩患者。
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
自引率
0.00%
发文量
0
期刊最新文献
[Action mechanism of antidepressive drugs. Review of current knowledge]. [Opsoclonus-ataxia syndrome. Description of a case]. [Neurological complications in Behçet's disease]. [Recited depression]. [Drop attack as the only symptom of type 1 Chiari malformation. Illustration by a case].
×
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