10, avenue Auguste-Renoir, 78160 Marly-le-Roi, France.
Int Orthod. 2024 Jun;22(2):100872. doi: 10.1016/j.ortho.2024.100872. Epub 2024 Apr 12.
The patient presented in this case report is a 10-year-old boy with hyperdivergent skeletal Class II associated with familial genetic agenesis of the second premolars. The treatment plan chosen was to close the spaces of agenesis using a bimaxillary appliance fixed buccally. The advantages and disadvantages of this treatment option were discussed. The result was stable and made it possible to avoid an implant-prosthetic solution, which would undoubtedly have been more restrictive over time.
本病例报告介绍了一位 10 岁男孩,其骨骼表现为高角型 II 类错颌畸形,伴第二前磨牙家族遗传性缺失。选择的治疗方案是使用双颌固定颊面管矫治器关闭缺失间隙。讨论了这种治疗方案的优缺点。结果稳定,避免了种植-修复解决方案,这无疑会随着时间的推移而更加受限。