Implant-Prosthetic Restoration of a Patient with Osteogenesis Imperfecta: A Case Report

被引:3
作者
Hanisch, Marcel [1 ]
Maus, Melanie [1 ]
Kleinheinz, Johannes [1 ]
机构
[1] Univ Hosp Munster, Res Unit Rare Dis Orofacial Manifestat, Dept Craniomaxillofacial Surg, Albert Schweitzer Campus 1,Bldg W30, D-48149 Munster, Germany
关键词
osteogenesis imperfecta; implant dentistry; oral health-related quality of life; rare diseases;
D O I
10.3390/ijerph18084169
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Osteogenesis imperfecta describes a group of genetic disorders that result from a defect in collagen type I and range in severity from a subtle increase in fracture frequency to death in the perinatal period. Osteogenesis imperfecta is mostly caused by mutations in the COL1A1 (17q21.33) and COL1A2 (7q21.3) genes. There have only been a few case reports of implant-prosthetic treatment for patients with osteogenesis imperfecta. These reports indicated that implants and augmentation procedures can be implemented in such patients. However, for patients receiving additional antiresorptive therapy, cautious approaches should be chosen and the risk of drug-associated osteonecrosis should be considered. The aim of this article is to report on the implant-prosthetic treatment of a patient with type I osteogenesis imperfecta.
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页数:7
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