A Rare Case of an Isolated Facial Nerve Aplasia: Radiological Findings

IF 1.4 Q3 PEDIATRICS Global Pediatric Health Pub Date : 2023-01-01 DOI:10.1177/2333794x231208365
Ola Messaoud, Kenza Horache, Amine Cherraqi, Fikri Meriem, Jiddane Mohamed, Touarsa Firdaous
{"title":"A Rare Case of an Isolated Facial Nerve Aplasia: Radiological Findings","authors":"Ola Messaoud, Kenza Horache, Amine Cherraqi, Fikri Meriem, Jiddane Mohamed, Touarsa Firdaous","doi":"10.1177/2333794x231208365","DOIUrl":null,"url":null,"abstract":"Congenital facial palsy is a rare condition that can be categorized into traumatic and developmental etiologies. Trauma related congenital facial palsy represents by far the most frequent cause with a spontaneous complete recovery within weeks, contrary to developmental causes that can be syndromic or non-syndromic, and have a poor prognosis. We present the case of an 11-month-old boy who suffers a congenital facial palsy. He undergoes an MRI examination with the adapted sequences to assess the facial nerve, and a high-resolution CT scan that reveals a seventh cranial nerve agenesis.","PeriodicalId":12576,"journal":{"name":"Global Pediatric Health","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global Pediatric Health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/2333794x231208365","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Congenital facial palsy is a rare condition that can be categorized into traumatic and developmental etiologies. Trauma related congenital facial palsy represents by far the most frequent cause with a spontaneous complete recovery within weeks, contrary to developmental causes that can be syndromic or non-syndromic, and have a poor prognosis. We present the case of an 11-month-old boy who suffers a congenital facial palsy. He undergoes an MRI examination with the adapted sequences to assess the facial nerve, and a high-resolution CT scan that reveals a seventh cranial nerve agenesis.
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
罕见孤立性面神经发育不全1例:影像学表现
先天性面瘫是一种罕见的疾病,可分为外伤性和发展性两种病因。迄今为止,创伤相关的先天性面瘫是最常见的原因,可在数周内自然完全恢复,而发展性原因可能是综合征性或非综合征性,预后较差。我们提出的情况下,一个11个月大的男孩谁遭受先天性面瘫。他接受了MRI检查,用适应的序列来评估面神经,并进行了高分辨率CT扫描,发现第七脑神经发育不全。
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
Global Pediatric Health
Global Pediatric Health Nursing-Pediatrics
CiteScore
2.20
自引率
0.00%
发文量
105
审稿时长
12 weeks
期刊最新文献
Children With Hepatitis in a Tertiary Care Center in Nepal: A Prospective Observational Study. Iron Deficiency Anemia and Dental Caries: A Systematic Review and Meta-Analysis. Chronic Conditions and Resilience: Adolescent Health Behaviors in the Midst of the COVID-19 Pandemic in Thailand. Early Neonatal Mortality and Predictors in Newborns Admitted to the Neonatal Intensive Care Unit at Public Hospitals in Hadiya Zone, Central Ethiopia: A Retrospective Cohort Study. Onset of Type I Diabetes Followed by Scleroderma Syndrome in a Child After the COVID-19: A Case Report.
×
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