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Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings

机译:成骨不全症及正畸和正颌联合手术:两个兄弟姐妹的病例报告

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摘要

Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal deformity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic surgery for the treatment of facial asymmetry and mandibular prognathism. The authors report two cases of combined orthodontics and orthognathic surgery in patients with type I osteogenesis imperfecta, mandibular prognathism, and facial asymmetry.
机译:成骨不全是结缔组织疾病的异质性组,主要特征是骨脆性和骨骼畸形。两名患有I型成骨不全症的未诊断兄弟姐妹接受正颌手术治疗面部不对称和下颌前突。作者报告了2例I型成骨不全症,下颌前突和面部不对称患者的正畸与正颌联合手术。

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