지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2020.1
- 수록면
- 70 - 77 (8page)
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초록· 키워드
오류제보하기
Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal de-formity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic surgery for the treatment of facial asymmetry and man-dibular 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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등록된 정보가 없습니다.
참고문헌 (20)
참고문헌 신청
Sillence DO / 1979 / Genetic heterogeneity in osteogenesis imperfecta / J Med Genet 16:101~116
Marini JC / 2007 / Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen : regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans / Hum Mutat 28:209~221
Körkkö J / 1998 / Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I : identification of common sequences of null-allele mutations / Am J Hum Genet 62:98~110
Tournis S / 2018 / Osteogenesis imperfecta : a clinical update / Metabolism 80:27~37
Rosén A / 2011 / Orthognathic bimaxillary surgery in two patients with osteogenesis imperfecta and a review of the literature / Int J Oral Maxillofac Surg 40:866~873
Marini JC / 2007 / Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen : regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans / Hum Mutat 28:209~221
Körkkö J / 1998 / Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I : identification of common sequences of null-allele mutations / Am J Hum Genet 62:98~110
Tournis S / 2018 / Osteogenesis imperfecta : a clinical update / Metabolism 80:27~37
Rosén A / 2011 / Orthognathic bimaxillary surgery in two patients with osteogenesis imperfecta and a review of the literature / Int J Oral Maxillofac Surg 40:866~873
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