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以单一下唇正中凹陷伴相关牙齿、口腔颌面及肢体畸形表现的范德伍德综合征:1例罕见病例报告

Van der Woude syndrome presenting as a single median lower lip pit with associated dental, orofacial and limb deformities: a rare case report.

作者信息

Richardson Sunil, Khandeparker Rakshit Vijay

机构信息

Richardsons Dental and Craniofacial Hospital, Nagercoil, India.

出版信息

J Korean Assoc Oral Maxillofac Surg. 2017 Aug;43(4):267-271. doi: 10.5125/jkaoms.2017.43.4.267. Epub 2017 Aug 24.

Abstract

Although it is a rare developmental malformation, van der Woude syndrome is the most common form of syndromic orofacial clefting, accounting for approximately 2% of all cleft cases. The lower lip pits with or without a cleft lip or palate is characteristic of the syndrome. Findings, such as hypodontia, limb deformities, popliteal webs, ankylogossia, ankyloblepheron, and genitourinary and cardiovascular abnormalities, are rarely associated with the syndrome. This paper reports a rare case of van der Woude syndrome in a 10-year-old male patient with a single median lower lip pit and a repaired bilateral cleft lip and cleft palate that were associated with microstomia, hypodontia, and clubbing of the left foot with syndactyly of the second to fifth lesser toes of the same foot.

摘要

尽管范德伍德综合征是一种罕见的发育畸形,但它是综合征性口面部裂隙最常见的形式,约占所有腭裂病例的2%。下唇凹陷伴或不伴有唇裂或腭裂是该综合征的特征。诸如牙量减少、肢体畸形、腘窝蹼、舌系带过短、睑裂狭小以及泌尿生殖系统和心血管系统异常等表现很少与该综合征相关。本文报告了一例罕见的范德伍德综合征病例,患者为一名10岁男性,有单个正中下唇凹陷以及已修复的双侧唇裂和腭裂,同时伴有小口畸形、牙量减少以及左脚杵状指并伴有同一侧第二至第五小趾并趾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14d5/5583202/fdd0a703261b/jkaoms-43-267-g002.jpg

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