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锁骨颅骨发育不全的牙科治疗策略

Dental treatment strategies in cleidocranial dysplasia.

作者信息

Jensen B L, Kreiborg S

机构信息

Institute of Paediatric Dentistry, Royal Dental College, Copenhagen.

出版信息

Br Dent J. 1992 Mar 21;172(6):243-7. doi: 10.1038/sj.bdj.4807836.

DOI:10.1038/sj.bdj.4807836
PMID:1554531
Abstract

Based on the findings of our recent longitudinal study on the abnormalities of the dentition in cleidocranial dysplasia (CCD), a hypothesis has been proposed, which makes it possible to predict time of onset of formation of supernumerary teeth and their location in the jaws. It was found that a diagnosis should be made early so that formation of supernumerary teeth can be diagnosed and early intervention undertaken. It should be possible to diagnose supernumerary incisors at about 5-7 years of age and supernumerary canines and premolars a few years later. When root length of the normal permanent teeth has reached about one third of its final length, the overlying supernumerary teeth should be removed, together with overlying bone and primary teeth. In regions where no supernumerary teeth are formed, eruption may also be improved by removal of the primary teeth and surgical exposure of the underlying permanent teeth. Conventional orthodontic treatment and eventually autotransplantation of teeth may still be necessary in the future, but it can be anticipated that the new strategy, with much earlier intervention, will materially reduce the extent of surgical and orthodontic interventions, which have previously been of extremely long duration, tedious to the patients and often of limited success.

摘要

基于我们最近关于锁骨颅骨发育不全(CCD)牙列异常的纵向研究结果,提出了一种假说,该假说能够预测多生牙的萌出时间及其在颌骨中的位置。研究发现应尽早做出诊断,以便能够诊断多生牙的形成并进行早期干预。大约在5至7岁时应能够诊断出多生切牙,几年后可诊断出多生尖牙和前磨牙。当正常恒牙的牙根长度达到其最终长度的约三分之一时,应将覆盖其上的多生牙连同覆盖的骨组织和乳牙一并拔除。在未形成多生牙的区域,拔除乳牙并手术暴露其下方的恒牙也可能改善萌出情况。未来可能仍需要常规正畸治疗以及最终的牙齿自体移植,但可以预期,这种早期干预的新策略将大大减少手术和正畸干预的程度,而此前这些干预持续时间极长,令患者厌烦且往往效果有限。

相似文献

1
Dental treatment strategies in cleidocranial dysplasia.锁骨颅骨发育不全的牙科治疗策略
Br Dent J. 1992 Mar 21;172(6):243-7. doi: 10.1038/sj.bdj.4807836.
2
Development of the dentition in cleidocranial dysplasia.锁骨颅骨发育不全患者牙列的发育
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[Development of the dentition in cleidocranial dysplasia].[锁骨颅骨发育不全患者牙列的发育]
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Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.罕见的 cleidocranial 发育不全患者多发性额外埋伏牙的遗传模式、正畸和外科治疗:病例报告。
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Cleidocranial dysplasia: diagnostic criteria and combined treatment.锁骨颅骨发育不全:诊断标准与综合治疗
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2
Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells.鉴定一个家族性颅骨锁骨发育不全症病例,并发现一个新的 RUNX2 突变,建立患者来源的诱导多能干细胞系。
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Case Rep Dent. 2020 Dec 19;2020:8910798. doi: 10.1155/2020/8910798. eCollection 2020.
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Autotransplantation in combination with orthodontic treatment.自体移植与正畸治疗相结合。
J Orthod Sci. 2019 Aug 8;8:11. doi: 10.4103/jos.JOS_62_18. eCollection 2019.
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Characterization of dental phenotype in patients with cleidocranial dysplasia using longitudinal data.利用纵向数据对颅锁骨发育不全患者的牙颌表型进行特征分析。
Angle Orthod. 2018 Jul;88(4):416-424. doi: 10.2319/092617-647.1. Epub 2018 Apr 17.
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Intractable Rare Dis Res. 2016 May;5(2):117-20. doi: 10.5582/irdr.2016.01022.
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