Absent Stapedius Muscle and other Rare Congenital Ossicular Anomalies: A Case Series

IF 0.2 Q4 OTORHINOLARYNGOLOGY Indian Journal of Otology Pub Date : 2022-04-01 DOI:10.4103/indianjotol.indianjotol_71_21
Madhukar Upadhyay, S. Goyal
{"title":"Absent Stapedius Muscle and other Rare Congenital Ossicular Anomalies: A Case Series","authors":"Madhukar Upadhyay, S. Goyal","doi":"10.4103/indianjotol.indianjotol_71_21","DOIUrl":null,"url":null,"abstract":"Conductive hearing loss due to ossicular anomalies is generally associated with external auditory canal dysplasia. Congenital ossicular anomalies in isolation are rare and often have a delayed diagnosis, particularly if unilateral. In such cases, the predominant symptom is conductive hearing loss and otosclerosis is usually the major differential diagnosis. We present a series of three cases of congenital ossicular chain anomaly. These patients were initially diagnosed as a case of otosclerosis. However, the diagnosis was revised based on intraoperative findings and managed accordingly.","PeriodicalId":44304,"journal":{"name":"Indian Journal of Otology","volume":"28 1","pages":"163 - 166"},"PeriodicalIF":0.2000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Otology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/indianjotol.indianjotol_71_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Conductive hearing loss due to ossicular anomalies is generally associated with external auditory canal dysplasia. Congenital ossicular anomalies in isolation are rare and often have a delayed diagnosis, particularly if unilateral. In such cases, the predominant symptom is conductive hearing loss and otosclerosis is usually the major differential diagnosis. We present a series of three cases of congenital ossicular chain anomaly. These patients were initially diagnosed as a case of otosclerosis. However, the diagnosis was revised based on intraoperative findings and managed accordingly.
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
足趾肌缺失及其他罕见先天性骨化异常:一系列病例
听骨异常引起的传导性听力损失通常与外耳道发育不良有关。孤立的先天性听骨异常是罕见的,往往有延迟诊断,特别是如果单侧。在这种情况下,主要症状是传导性听力丧失,耳硬化通常是主要的鉴别诊断。我们报告三例先天性听骨链异常。这些病人最初被诊断为耳硬化症。然而,根据术中发现对诊断进行了修改并进行了相应的处理。
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
Indian Journal of Otology
Indian Journal of Otology OTORHINOLARYNGOLOGY-
CiteScore
0.40
自引率
0.00%
发文量
21
期刊最新文献
Comparative study between anterior tucking and tunneling of graft in Type-1 tympanoplasty A comparative study of endoscopic versus microscopic tympanoplasty in chronic otitis media Application of finite element model of middle ear in the study of the middle ear biomechanics in normal and diseased states Transmastoid titanium mesh assisted extra dural layered closure of tegmen defect: Case report in a 10 year old Acoustic trauma in soldiers: Pure-tone audiometry versus distortion product otoacoustic emissions as a tool for early detection
×
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