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本文引用的文献

1
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.丹麦一个五代家系中低钙性牙本质发育不全的表型变异有限,该家系存在一个新型 FAM83H 无义突变。
Int J Paediatr Dent. 2011 Nov;21(6):407-12. doi: 10.1111/j.1365-263X.2011.01142.x. Epub 2011 Jun 27.
2
Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.牙釉质不全患者的颅面特征和基因型。
Eur J Orthod. 2011 Jun;33(3):325-31. doi: 10.1093/ejo/cjq089. Epub 2010 Nov 10.
3
A multidisciplinary approach to the functional and esthetic rehabilitation of amelogenesis imperfecta and open bite deformity: a case report.多学科方法治疗牙釉质发育不全和开颌畸形的功能和美观修复:病例报告。
J Esthet Restor Dent. 2010 Oct;22(5):282-93. doi: 10.1111/j.1708-8240.2010.00354.x.
4
Interdisciplinary treatment of a patient with amelogenesis imperfecta, a skeletal Class III relationship, and an anterior open bite.对一名患有牙釉质发育不全、骨性Ⅲ类错牙合关系和前牙开牙合的患者进行多学科治疗。
World J Orthod. 2010 Fall;11(3):284-90.
5
Cone-rod dystrophy and amelogenesis imperfecta (Jalili syndrome): phenotypes and environs. Cone-rod 营养不良和牙本质发育不全(Jalili 综合征):表型和环境。
Eye (Lond). 2010 Nov;24(11):1659-68. doi: 10.1038/eye.2010.103. Epub 2010 Aug 13.
6
Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.因釉原蛋白基因突变导致的釉质发育不全:基因型与表型相关性的临床病例
Pediatr Dent. 2010 Jan-Feb;32(1):56-60.
7
Restoring function and aesthetics in a patient previously treated for amelogenesis imperfecta.恢复一名曾接受过釉质发育不全治疗患者的功能和美观。
Eur J Prosthodont Restor Dent. 2009 Dec;17(4):170-6.
8
A conservative treatment for amelogenesis imperfecta with direct resin composite restorations: a case report.采用直接树脂复合材料修复治疗牙釉质发育不全的保守疗法:病例报告
J Esthet Restor Dent. 2009;21(3):161-9; discussion 170. doi: 10.1111/j.1708-8240.2009.00258.x.
9
Amelogenesis imperfecta - a systematic literature review of associated dental and oro-facial abnormalities and their impact on patients.牙釉质发育不全——关于相关牙齿及口腔面部异常及其对患者影响的系统文献综述
Acta Odontol Scand. 2008 Aug;66(4):193-9. doi: 10.1080/00016350802192071.
10
Enamel dysplasia with hamartomatous atypical follicular hyperplasia (EDHFH) syndrome: suggested pathogenic mechanisms.伴有错构瘤性非典型滤泡增生的釉质发育不全(EDHFH)综合征:推测的致病机制。
SADJ. 2008 Mar;63(2):102-5.

牙釉质发育不全与前牙开颌:病因、分类、临床及治疗的相互关系

Amelogenesis imperfecta and anterior open bite: Etiological, classification, clinical and management interrelationships.

作者信息

Alachioti Xanthippi Sofia, Dimopoulou Eleni, Vlasakidou Anatoli, Athanasiou Athanasios E

机构信息

Department of Orthodontics, Faculty of Dentistry, School of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.

Department of Orthodontics, Faculty of Dentistry, School of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece ; Dubai School of Dental Medicine, Dubai, United Arab Emirates.

出版信息

J Orthod Sci. 2014 Jan;3(1):1-6. doi: 10.4103/2278-0203.127547.

DOI:10.4103/2278-0203.127547
PMID:24987656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4072389/
Abstract

Although amelogenesis imperfecta is not a common dental pathological condition, its etiological, classification, clinical and management aspects have been addressed extensively in the scientific literature. Of special clinical consideration is the frequent co-existence of amelogenesis imperfecta with the anterior open bite. This paper provides an updated review on amelogenesis imperfecta as well as anterior open bite, in general, and documents the association of these two separate entities, in particular. Diagnosis and treatment of amelogenesis imperfecta patients presenting also with anterior open bite require a lengthy, comprehensive and multidisciplinary approach, which should aim to successfully address all dental, occlusal, developmental, skeletal and soft tissue problems associated with these two serious clinical conditions.

摘要

尽管牙釉质发育不全并非常见的牙齿病理状况,但其病因、分类、临床及治疗方面在科学文献中已有广泛论述。牙釉质发育不全常与前牙开合并存,这一点在临床中尤其值得关注。本文对牙釉质发育不全以及前牙开合进行了全面的综述,并特别记录了这两种独立病症之间的关联。对同时患有牙釉质发育不全和前牙开合的患者进行诊断和治疗,需要采取长期、全面且多学科的方法,旨在成功解决与这两种严重临床病症相关的所有牙齿、咬合、发育、骨骼及软组织问题。