• 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

伴有面部不对称的最常见先天性综合征:一项叙述性综述。

Most common congenital syndromes with facial asymmetry: A narrative review.

作者信息

Paradowska-Stolarz Anna Maria, Ziomek Marta, Sluzalec-Wieckiewicz Katarzyna, Duś-Ilnicka Irena

机构信息

Division of Facial Developmental Defects, Department of Maxillofacial Orthopaedics and Orthodontics, Wroclaw Medical University, Poland.

Faculty of Dentistry, Wroclaw Medical University, Poland.

出版信息

Dent Med Probl. 2024 Nov-Dec;61(6):925-932. doi: 10.17219/dmp/186086.

DOI:10.17219/dmp/186086
PMID:39496100
Abstract

Symmetry is present in various aspects of everyday life. A symmetrical face is considered attractive, whereas a lack of facial symmetry is regarded as a source of functional and aesthetic problems. Most of the people exhibit slight asymmetries, but some of them reveal severe asymmetries. Among patients presenting with severe facial asymmetries, there may be those with congenital defects. Congenital defects may manifest at the time of birth or be a result of birth trauma.One of the most prevalent asymmetrical birth defects is cleft lip and/or cleft palate. Other congenital defects include craniofacial syndromes, such as Treacher Collins syndrome (TCS) and Goldenhar syndrome. Among the rare syndromes with facial asymmetries, Klippel-Feil syndrome (KFS), PHACE (posterior fossa brain malformation, hemangiomas, arterial anomalies, cardiac anomalies, and eye abnormalities) syndrome, plagiocephaly, and Parry-Romberg syndrome are worth noticing. The majority of craniofacial asymmetries require surgery to improve the patient's facial appearance. The treatment is multidisciplinary and long, and the most common procedures involve reparative and regenerative surgeries. The aim of this review was to present the most common congenital defects with facial asymmetry.

摘要

对称性存在于日常生活的各个方面。对称的面部被认为具有吸引力,而面部不对称则被视为功能和美学问题的根源。大多数人表现出轻微的不对称,但其中一些人则存在严重的不对称。在患有严重面部不对称的患者中,可能有先天性缺陷者。先天性缺陷可能在出生时就表现出来,或者是出生创伤的结果。最常见的不对称出生缺陷之一是唇裂和/或腭裂。其他先天性缺陷包括颅面综合征,如特雷彻·柯林斯综合征(TCS)和戈尔登哈综合征。在罕见的面部不对称综合征中,克利佩尔-费尔综合征(KFS)、PHACE(后颅窝脑畸形、血管瘤、动脉异常、心脏异常和眼部异常)综合征、扁头畸形和帕里-罗姆伯格综合征值得关注。大多数颅面不对称需要手术来改善患者的面部外观。治疗是多学科且漫长的,最常见的手术包括修复性和再生性手术。本综述的目的是介绍最常见的伴有面部不对称的先天性缺陷。

相似文献

1
Most common congenital syndromes with facial asymmetry: A narrative review.伴有面部不对称的最常见先天性综合征:一项叙述性综述。
Dent Med Probl. 2024 Nov-Dec;61(6):925-932. doi: 10.17219/dmp/186086.
2
The treatment of facial asymmetry: Review.
Adv Clin Exp Med. 2017 Nov;26(8):1301-1311. doi: 10.17219/acem/68976.
3
Composite tissue allotransplantation for the reconstruction of congenital craniofacial defects.用于先天性颅面缺损重建的复合组织同种异体移植
Transplant Proc. 2009 Mar;41(2):523-7. doi: 10.1016/j.transproceed.2009.01.016.
4
Goldenhar syndrome and hemifacial microsomia: observations on three patients.戈尔登哈综合征与半侧颜面短小畸形:三例患者观察报告
Eur J Pediatr. 1980 May;133(3):287-92. doi: 10.1007/BF00496092.
5
Facial asymmetries in hemifacial microsomia, Goldenhar syndrome, and Treacher Collins syndrome.半侧颜面短小畸形、Goldenhar综合征和Treacher Collins综合征中的面部不对称。
Atlas Oral Maxillofac Surg Clin North Am. 1996 Mar;4(1):37-52.
6
Single-stage Repair of Bilateral Cleft Lip and Bilateral Transverse Facial Cleft in Goldenhar Syndrome: A Case Report.单侧完全性唇裂和双侧下颌面裂综合征的一期修复:病例报告。
Cleft Palate Craniofac J. 2023 Nov;60(11):1513-1516. doi: 10.1177/10556656231161990. Epub 2023 Jul 13.
7
[Epidemiology of orofacial clefts (1995-2006) in France (Congenital Malformations of Alsace Registry)].[法国(阿尔萨斯先天性畸形登记处)口面部裂隙的流行病学研究(1995 - 2006年)]
Arch Pediatr. 2012 Oct;19(10):1021-9. doi: 10.1016/j.arcped.2012.07.002. Epub 2012 Aug 24.
8
Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention.颅面出生缺陷:神经嵴细胞在特雷彻·柯林斯综合征的病因和发病机制中的作用以及预防的潜力。
Am J Med Genet A. 2010 Dec;152A(12):2984-94. doi: 10.1002/ajmg.a.33454. Epub 2010 Aug 23.
9
Congenital anomalies associated with cleft lip and palate-an analysis of 1623 consecutive patients.唇腭裂相关先天性畸形——1623例连续病例分析
Cleft Palate Craniofac J. 2011 Jul;48(4):371-8. doi: 10.1597/09-264. Epub 2010 Jul 1.
10
Multidisciplinary treatment approach in Treacher Collins syndrome.特雷彻·柯林斯综合征的多学科治疗方法。
J Dent Child (Chic). 2012 Jan-Apr;79(1):15-21.

引用本文的文献

1
A new objective titration procedure using Remotely Contactless Intelligent Sleep Monitoring System for the treatment of mandibular advancement device in OSAHS patient.一种使用远程非接触式智能睡眠监测系统的新客观滴定程序,用于治疗阻塞性睡眠呼吸暂停低通气综合征(OSAHS)患者的下颌前移装置。
Front Neurol. 2025 Jul 18;16:1631296. doi: 10.3389/fneur.2025.1631296. eCollection 2025.
2
Obstructive Sleep Apnoea in Patients with Treacher Collins Syndrome-A Narrative Review.特雷彻·柯林斯综合征患者的阻塞性睡眠呼吸暂停——一项叙述性综述
J Clin Med. 2025 Jul 4;14(13):4741. doi: 10.3390/jcm14134741.
3
Oral Implications of Herbst Device Modification: A Case Report.
Herbst矫治器改良的口腔影响:一例报告
Children (Basel). 2025 Apr 22;12(5):531. doi: 10.3390/children12050531.
4
Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic Overview.综合征型和非综合征型原发性牙齿萌出失败:遗传学概述。
Genes (Basel). 2025 Jan 24;16(2):147. doi: 10.3390/genes16020147.