《口腔颌面外科杂志》 ›› 2023, Vol. 33 ›› Issue (5): 350-353. doi: 10.12439/kqhm.1005-4979.2023.05.014

• 病例报告 • 上一篇    

颅锁骨发育不全1例并文献复习

柴安1(), 雷荣昌2(), 曲彬彬2, 李鹤2, 邵奇2, 蒋智升2   

  1. 1 湖南中医药大学研究生院,长沙 410000
    2 长沙市口腔医院口腔颌面外科,长沙 410004
  • 收稿日期:2022-06-14 接受日期:2022-12-08 出版日期:2023-10-28 发布日期:2023-11-03
  • 通讯作者: 雷荣昌,主任医师. E-mail:leroch@163.com
  • 作者简介:
    柴安,硕士研究生. E-mail:

Cleidocranial dysplasia: Case report and literature review

CHAI An1(), LEI Rongchang2(), QU Binbin2, LI He2, SHAO Qi2, JIANG Zhisheng2   

  1. 1 Hunan University of Chinese Medicine, Graduate School, Changsha 410000
    2 Department of Oral and Maxillofacial Surgery, Changsha Stomatological Hospital, Changsha 410004, China
  • Received:2022-06-14 Accepted:2022-12-08 Online:2023-10-28 Published:2023-11-03

摘要:

颅锁骨发育不全(cleidocranial dysplasia, CCD)较为少见,通常因口腔问题就诊时而被发现。临床上需尽早完善此类病例的相关检查,对口腔颌面部问题进行处理,以便重建稳定的咬合关系,提高生活质量。本文报告1例CCD,并结合其治疗过程进行文献回顾,总结该病的临床表现、病因、诊断、治疗等特点。

关键词: 颅锁骨发育不全, 基因突变, 正畸-正颌联合治疗, 多生牙

Abstract:

Cleidocranial dysplasia (CCD) is rare, which was usually found accidentally when they consulted a doctor due to oral problems. Clinically, it is necessary to improve relevant examinations and deal with oral and maxillofacial problems for such cases. It is essential to rebuild a stable occlusal relationship and improve the quality of life. This paper reports a rare case of CCD and reviews the current literature on the clinical manifestations、etiology、diagnosis and various treatment modalities of this disease.

Key words: cleidocranial dysplasia, genetic mutation, orthodontic and orthognathic combined treatment, supernumerary tooth

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