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牙本质发育不全Ⅱ型患者的重建治疗 被引量:2

Occlusal reconstruction for patients with dentinogenesis imperfecta typeⅡ
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摘要 目的对牙本质发育不全Ⅱ型(DG I-Ⅱ)患者进行重建修复,观察疗效并总结修复要点。方法收集1个DG I-Ⅱ的家系资料,对先证者(患者1,女性,21岁)及其亲属(患者2,男性,40岁)的临床特征、修复过程和随访情况进行回顾性分析。结果 2例DG I-Ⅱ患者均以牙列重度磨耗为主要特征,其中患者2伴上下牙列缺损。患者1经重建、冠延长后行烤瓷固定修复;患者2经重建后以可摘局部义齿修复。修复后1年进行随访,患者主观感觉和临床检查均显示美观及咀嚼和发音功能均得到明显改善。结论 DG I-Ⅱ的修复应以阻断磨损及重建咬为原则,在重建基础上的固定或可摘局部义齿修复效果良好。 Objective To perform occlusal reconstruction for patients with dentinogenesis imperfecta type Ⅱ(DGI-Ⅱ),observe the clinic effect and summarize the clinical experience. Methods The data of one family of DGI-Ⅱ were collected,and the clinical characteristics,treatment process and follow-up status of the proband(patient 1,female,21 years old) and her relative(patient 2,male,40 years) were retrospectively analysed. Results The main feature of these two cases of DGI-Ⅱ was severe wear of the dentition,including upper and lower dentition defect in patient 2.After occlusal reconstruction and crown lengthening,patient 1 was restored by ceramic fixed partial denture to reconstruct the occlusion.Patient 2 was restored by removal partial denture after occlusal reconstruction.Patients were followed up 1 year after prosthetic treatment,and the subjective feelings of patients and clinical examinations indicated that the esthetics,mastication function and pronunciation of patients were significantly improved. Conclusion The principle of prosthetic treatment of patients with DGI-Ⅱ should be occlusal reconstruction of worn dentition.Occlusal reconstruction in combination with fixed or removable partial denture may yield favorable clinic effect.
出处 《上海交通大学学报(医学版)》 CAS CSCD 北大核心 2011年第7期1050-1054,共5页 Journal of Shanghai Jiao tong University:Medical Science
基金 上海市科委基金(08DZ2271100) 上海市重点(特色)学科建设项目(T0202)~~
关键词 牙本质发育不全Ⅱ型 遗传性 修复 (牙合)重建 dentinogenesis imperfecta type Ⅱ hereditary restoration occlusal reconstruction
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  • 1李长福,高山,刘萍,王晨.遗传性乳光牙本质牙体元素成分的分析[J].现代口腔医学杂志,2001,15(5):332-333. 被引量:6
  • 2Jung-Wook Kim,Jan C-C Hu,Jae-Il Lee,Sung-Kwon Moon,Young-Jae Kim,Ki-Taeg Jang,Sang-Hoon Lee,Chong-Chul Kim,Se-Hyun Hahn,James P. Simmer.Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II[J]. Human Genetics . 2005 (3)
  • 3Kindelan J,Tobin M,Roberts-Harry D,et al.Orthodontic andorthognathic management of a patient with osteogenesis im-perfectaand dentinogenesis imperfecta:a case report. J Orthod . 2003
  • 4Battagel JM,Levinkind M.Dentinogenesis imperfecta:an interdis-ciplinary approach. British Dental Journal . 1988
  • 5Zlotogora J,Fuks A,Borochowitz Z,et al.Kohlschtter-T nzsyndrome:epilepsy,dementia,and amelogenesis imperfecta. American Journal of Medical Genetics . 1993
  • 6Darendeliler-Kaba A,Maréchaux SC.Hereditary dentinogenesisimperfecta:a treatment program using an overdenture. ASOC JDent Child . 1992
  • 7Roh WJ,Seung-Goo Kang SG,Kim SJ.Multidisciplinary approachfor a patient with dentinogenesis imperfecta and anterior trauma. American Journal of Orthodontics and Dentofacial Orthopedics . 2010
  • 8Wismeijer D,van Waas MA,Kalk W.Factors to consider in selec-ting an occlusal concept for patients with implants in the edentulousmandible. The Journal of ProsThetic Dentistry . 1995
  • 9Michael D. Crowell DDS MS.Dentinogenesis imperfecta: A case report. American Journal of Orthodontics and Dentofacial Orthopedics . 1998
  • 10Rajpar MH,Koch MJ,Davies RM,et al.Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization. Human Molecular Genetics . 2002

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同被引文献14

  • 1拜红霞,崔英霞.遗传性牙本质发育不全Ⅱ型的疾病基因研究进展[J].中国优生与遗传杂志,2006,14(1):115-116. 被引量:5
  • 2樊明文.牙体牙髓病学[M].北京:人民卫生出版社,2002.226.
  • 3Witkop CJ. Hereditary defects in enamel and dentin[ J ]. Acta Genet Star Med, 1957,7( 1 ) :236-239.
  • 4Roberts E, Schour I. Hereditary opalescent dentine ( dentinogenesis imperfeeta) [J]. Am J Orthod Oral Surg, 1939,25(3) :267-276.
  • 5Shields ED, Bixler D, EI-Kafrawy AM. A proposed classification for heritable human dentine defects with a description of a new entity [J]. Arch Oral Biol, 1973,18(4) :543-553.
  • 6Dean JA, Hartsfield Jr JK, Wright JT, et al. Dentin dysplasia, type Ⅱ linkage to chromosome 4q [ J ]. J Craniofac Genet Dev Biol, 1997, 17(4) :172-177.
  • 7齐艳珍,方会英.金瓷全冠修复遗传性乳光牙本质1例[J].口腔舱面修复学杂志,2006,7(4):295-295.
  • 8Gough MB, Setchell DJ. A retrospeetive study of 50 treat- ments using an appliance to produce localised occlusal space by relative axial tooth movement [ J]. Br Dent J, 1999, 187 (3): 134-139.
  • 9Poyser N J, Porter RW, Briggs PF, et al. The Dahl Con- cept : Past, present and future [ J ]. Br Dent J, 2005, 198 ( 11 ) : 669 - 676.
  • 10Redman CD, Hemmings KW, Good JA. The survival and clinical performance of resin-based eomposite restorations used to treat localised anterior tooth wear [ J]. Br Dent J, 2003, 194 (10) : 566 -572.

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