口腔医学研究 ›› 2024, Vol. 40 ›› Issue (8): 741-743.DOI: 10.13701/j.cnki.kqyxyj.2024.08.014

• 病例报告 • 上一篇    下一篇

颅骨锁骨发育不全综合征伴17颗多生牙1例

郭龙妹, 韩久松*   

  1. 南方医科大学口腔医院口腔颌面外科 广东 广州 510280
  • 收稿日期:2023-09-25 出版日期:2024-08-28 发布日期:2024-08-22
  • 通讯作者: *韩久松,E-mail:hanjiusong@126.com
  • 作者简介:郭龙妹(1993~ ),女,广东人,住院医师,硕士,研究方向:儿童口腔与固定矫治器研究等。

A Case Report of Cleidocranial Dysplasia with 17 Supernumerary Teeth

GUO Longmei, HAN Jiusong*   

  1. Department of Oral and Maxillofacial Surgery, Stomatological Hospital, Southern Medical University, Guangzhou 510280, China
  • Received:2023-09-25 Online:2024-08-28 Published:2024-08-22

摘要: 颅骨锁骨发育不全综合征是一种少见的先天性骨骼和牙齿发育不良综合征,伴10颗以上多生牙罕见。本文报道1例颅骨锁骨发育不全综合征伴17颗埋伏多生牙的临床和放射检查结果以及多生牙拔除的治疗过程。

关键词: 多生牙, 颅骨锁骨发育不全综合征, 多发性

Abstract: Cleidocranial dysplasia (CCD) is a rare congenital disorder that primarily affects the development of bones and teeth, especially unusual with more than 10 supernumerary teeth. This article reports the clinical and radiological findings of a case of CCD with 17 impacted supplementary teeth, also comprises the procedure of the surgical extraction of the supernumerary teeth.

Key words: supernumerary teeth, cleidocranial dysplasia, multiple