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Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings
Article in En | WPRIM | ID: wpr-811266
Responsible library: WPRO
ABSTRACT
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.
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Full text: 1 Index: WPRIM Main subject: Orthodontics / Osteogenesis / Osteogenesis Imperfecta / Prognathism / Congenital Abnormalities / Connective Tissue Diseases / Siblings / Facial Asymmetry / Orthognathic Surgery Limits: Humans Language: En Journal: Journal of the Korean Association of Oral and Maxillofacial Surgeons Year: 2020 Type: Article
Full text: 1 Index: WPRIM Main subject: Orthodontics / Osteogenesis / Osteogenesis Imperfecta / Prognathism / Congenital Abnormalities / Connective Tissue Diseases / Siblings / Facial Asymmetry / Orthognathic Surgery Limits: Humans Language: En Journal: Journal of the Korean Association of Oral and Maxillofacial Surgeons Year: 2020 Type: Article