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病例报告:一名牙本质发育不全且先天性侧切牙缺失儿童的康复治疗

Case report: Rehabilitation of a child with dentinogenesis imperfecta and congenitally missing lateral incisors.

作者信息

Millet C, Viennot S, Duprez J P

机构信息

Department of Prosthodontics School of Dentistry, University Lyon I, Faculté d'Odontologie, Rue Guillaume Paradin, 69372 Lyon Cedex 08, France.

出版信息

Eur Arch Paediatr Dent. 2010 Oct;11(5):256-60. doi: 10.1007/BF03262758.

DOI:10.1007/BF03262758
PMID:20932402
Abstract

BACKGROUND

Dentinogenesis imperfecta is one of the most common hereditary disorders of dentine formation. Opalescent teeth composed of irregularly formed and undemineralised dentine that obliterates pulp chambers and root canals characterize it. Complete-coverage crowns are usually the preferred restoration for patients with this condition.

CASE REPORT

A 9 year-old girl presented with dentinogenesis imperfecta, congenitally missing maxillary lateral incisors and maxillary right permanent second molar retention.

TREATMENT

The treatment comprised an initial approach to allow the correct eruption of the retained second molar. The use of low-fusion metal ceramic restorations comprised a second stage to improve the aesthetic appearance and decrease the risk of overload on teeth with limited value.

FOLLOW-UP: The patient has been recalled regularly and at the last visit, 10 years after initial prosthetic treatment, no problems or signs of complications have occurred. The patient is now aged 25 years and is still satisfied with the prosthetic rehabilitation.

CONCLUSION

This case illustrates the need for appropriate and timely restorative treatment to prevent deterioration of the dentition. This case will also demonstrate that low-fusion metal ceramic restoration is a viable esthetic treatment option for today's patients.

摘要

背景

牙本质发育不全是牙本质形成最常见的遗传性疾病之一。其特征为牙齿呈乳光色,由不规则形成且未脱矿的牙本质组成,牙髓腔和根管被其充填。对于患有这种疾病的患者,全冠修复通常是首选的修复方式。

病例报告

一名9岁女孩患有牙本质发育不全,上颌侧切牙先天性缺失,上颌右侧恒第二磨牙滞留。

治疗

治疗首先采取措施使滞留的第二磨牙正确萌出。第二阶段采用低熔金属烤瓷修复体,以改善美观并降低对价值有限的牙齿造成过载的风险。

随访

患者定期复诊,在首次修复治疗10年后的最后一次复诊时,未出现任何问题或并发症迹象。患者现25岁,仍对修复治疗效果满意。

结论

该病例表明需要进行适当及时的修复治疗以防止牙列恶化。该病例还将证明,低熔金属烤瓷修复对于当今患者而言是一种可行的美学治疗选择。

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A novel approach to full-mouth rehabilitation of dentinogenesis imperfecta type II: Case series with review of literature.一种治疗牙本质生成不全 II 型的全口修复新方法:病例系列及文献复习。
Medicine (Baltimore). 2024 Jan 26;103(4):e36882. doi: 10.1097/MD.0000000000036882.

本文引用的文献

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Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study.成骨不全症患儿的牙本质生成不全:临床和超微结构研究。
Int J Paediatr Dent. 2010 Mar;20(2):112-8. doi: 10.1111/j.1365-263X.2010.01033.x.
2
Survival rates of all-ceramic systems differ by clinical indication and fabrication method.全瓷系统的存活率因临床适应证和制作方法而异。
J Evid Based Dent Pract. 2010 Mar;10(1):37-8. doi: 10.1016/j.jebdp.2009.11.013.
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De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.
日本一个家族中与II型牙本质发育不全相关的DSPP基因的新发突变。
Eur J Oral Sci. 2009 Dec;117(6):691-4. doi: 10.1111/j.1600-0722.2009.00683.x.
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Complex all-ceramic rehabilitation of a young patient with a severely compromised dentition: a case report.一名牙列严重受损的年轻患者的复杂全瓷修复:病例报告
Quintessence Int. 2009 Jan;40(1):19-27.
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[Agenesis of the maxillary lateral incisors: orthodontic and implant approach].[上颌侧切牙先天缺失:正畸与种植治疗方法]
Orthod Fr. 2008 Dec;79(4):283-93. doi: 10.1051/orthodfr:2008020. Epub 2008 Dec 9.
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Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.遗传性牙本质疾病:牙本质发育不全和牙本质发育异常。
Orphanet J Rare Dis. 2008 Nov 20;3:31. doi: 10.1186/1750-1172-3-31.
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Dentinogenesis imperfecta: long-term rehabilitation in a child.牙本质发育不全:一名儿童的长期康复治疗
J Dent Child (Chic). 2008 May-Aug;75(2):192-6.
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Dentinogenesis imperfecta: the importance of early treatment.牙本质发育不全:早期治疗的重要性。
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Dentinogenesis imperfecta type II: an affected family saga.II型牙本质发育不全:一个患病家族的故事
J Oral Sci. 2007 Sep;49(3):241-4. doi: 10.2334/josnusd.49.241.
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Rehabilitation of a patient with amelogenesis imperfecta using all-ceramic crowns: a clinical report.使用全瓷冠修复牙釉质发育不全患者:临床报告
J Prosthet Dent. 2007 Aug;98(2):85-8. doi: 10.1016/S0022-3913(07)60041-9.