• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Clinical analysis of 592 patients with microtia.

作者信息

Okajima H, Takeichi Y, Umeda K, Baba S

机构信息

Department of Otorhinolaryngology, Nagoya City University Medical School, Japan.

出版信息

Acta Otolaryngol Suppl. 1996;525:18-24.

PMID:8908264
Abstract

Clinical and statistical analyses were performed on 592 patients who visited our hospital between April 1968 and March 1995. The preponderance in men (64.7%) and right-side (58.4%) was distinct statistically. The material shows that grade III microtia, peanut-shell type, was the most frequent with 56.8%. It is complicated with congenital stenosis or atresia in most cases (92.0%). The degree of anomalies of the auricle and external auditory meatus was generally interrelated. Ten cases of familial microtia were discovered, and all parent-child cases were father-child. About 27.9% of the patients' mothers had had a cold, threatened abortion, gestosis, anemia, etc during their pregnancy. Except for 6 patients with Treacher-Collin's syndrome and 2 patients whose mothers took thalidomide during pregnancy, we could not demonstrate the cause of the microtia, whether general or environmental.

摘要

相似文献

1
Clinical analysis of 592 patients with microtia.
Acta Otolaryngol Suppl. 1996;525:18-24.
2
Correlation between microtia and temporal bone malformation evaluated using grading systems.使用分级系统评估小耳畸形与颞骨畸形之间的相关性。
Arch Otolaryngol Head Neck Surg. 2005 Apr;131(4):326-9. doi: 10.1001/archotol.131.4.326.
3
[Epidemiology and risk factors for microtia in Colombia].[哥伦比亚小耳畸形的流行病学及危险因素]
Acta Otorrinolaringol Esp. 2009 Mar-Apr;60(2):115-9.
4
[Microtia--not just an ear problem].[小耳畸形——不仅仅是耳朵的问题]
Duodecim. 2009;125(9):975-82.
5
Epidemiological analysis of microtia: a retrospective study in 345 patients in China.
Int J Pediatr Otorhinolaryngol. 2010 Mar;74(3):275-8. doi: 10.1016/j.ijporl.2009.12.001. Epub 2009 Dec 29.
6
[Clinico-epidemiologic study of microtia].[小耳畸形的临床流行病学研究]
Invest Clin. 1997 Dec;38(4):203-17.
7
Microtia in Finland: comparison of characteristics in different populations.芬兰的小耳畸形:不同人群特征比较
Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1211-7. doi: 10.1016/j.ijporl.2007.04.020. Epub 2007 Jun 4.
8
Familial microtia in four generations with variable expressivity and incomplete penetrance in association with type I syndactyly.四代家族性小耳畸形,具有可变表达和不完全外显率,并伴有I型并指畸形。
Turk J Pediatr. 2001 Oct-Dec;43(4):362-5.
9
[Surgery of juvenile external ear abnormalities].[青少年外耳畸形的外科治疗]
Laryngol Rhinol Otol (Stuttg). 1984 Mar;63(3):120-2.
10
[Reconstruction of the floor of the auricle in congenital microtia in children].
Vestn Otorinolaringol. 1996 Sep-Oct(5):24-6.

引用本文的文献

1
Epidemiological Characteristics and Maternal Risk Factors of Microtia and Aural Atresia in Kazakhstan.哈萨克斯坦小耳畸形和外耳道闭锁的流行病学特征及母体危险因素
Int Arch Otorhinolaryngol. 2025 Jan 27;29(1):1-8. doi: 10.1055/s-0044-1792015. eCollection 2025 Jan.
2
The role of MRI in the prenatal diagnosis and classification of fetal microtia.MRI 在胎儿小耳畸形的产前诊断和分类中的作用。
Eur Radiol. 2023 Nov;33(11):7707-7715. doi: 10.1007/s00330-023-09816-5. Epub 2023 Jun 14.
3
Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect.
22q11.2 号染色体靶向区域的基因筛查在小耳畸形和先天性心脏病患者中的应用。
Genes (Basel). 2023 Apr 7;14(4):879. doi: 10.3390/genes14040879.
4
Predicting the Risk of Microtia From Prenatal Factors: A Hospital-Based Case-Control Study.基于医院的病例对照研究:从产前因素预测小耳畸形的风险
Front Pediatr. 2022 Apr 21;10:851872. doi: 10.3389/fped.2022.851872. eCollection 2022.
5
Microtia: A Data Linkage Study of Epidemiology and Implications for Service Delivery.小耳畸形:一项关于流行病学及服务提供影响的数据关联研究。
Front Pediatr. 2021 Mar 26;9:630036. doi: 10.3389/fped.2021.630036. eCollection 2021.
6
DNA Methylation Patterns of Chronic Explosive Breaching in U.S. Military Warfighters.美国军事作战人员慢性爆炸伤的DNA甲基化模式
Front Neurol. 2020 Oct 23;11:1010. doi: 10.3389/fneur.2020.01010. eCollection 2020.
7
Sociodemographic, health behavioral, and clinical risk factors for anotia/microtia in a population-based case-control study.一项基于人群的病例对照研究中无耳/小耳畸形的社会人口学、健康行为和临床危险因素。
Int J Pediatr Otorhinolaryngol. 2019 Jul;122:18-26. doi: 10.1016/j.ijporl.2019.03.026. Epub 2019 Mar 23.
8
Identification of sequence variants associated with severe microtia-astresia by targeted sequencing.通过靶向测序鉴定与严重小耳畸形-无耳症相关的序列变异。
BMC Med Genomics. 2019 Jan 28;12(1):28. doi: 10.1186/s12920-019-0475-x.
9
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia.对307个耳聋基因进行靶向测序,确定了与小耳畸形相关的候选基因。
Oncotarget. 2017 Jun 28;8(38):63324-63332. doi: 10.18632/oncotarget.18803. eCollection 2017 Sep 8.
10
Genetic Advances in the Understanding of Microtia.耳郭畸形认识中的遗传学进展
J Pediatr Genet. 2016 Dec;5(4):189-197. doi: 10.1055/s-0036-1592422. Epub 2016 Sep 23.