单词osteogenesis imperfecta
网络: 成骨不全症
Osteogenesis imperfecta (OI) is an inherited disease where basic pathology is of defective maturation of collagen.
成骨不全症（着）是一种遗传性疾病的基本病理是在有缺陷的成熟的胶原质。
Osteogenesis imperfecta is an inherited disorder of connective tissue, which affects the skeleton, ligament, skin, sclera, and dentin.
骨发生不全是一种遗传性的结缔组织病变，常侵犯骨骼、韧带、皮肤、角膜及牙齿。
After diagnosis, she was suffering from the rare "typical osteogenesis imperfecta" , which is the first in the Southwest fairly.
经诊断，她患上的是罕见的“典型成骨不全症”，这在西南地区还算是首例。
Objective To summarize the experience of pamidronate for osteogenesis imperfecta.
目的总结帕米膦酸钠在成骨不全症中的应用经验。
Study Design. We report 2 cases of acute cervical compression fracture in patients with osteogenesis imperfecta (OI).
研究设计：我们报告2例成骨不全（OI）患者急性颈椎压缩性骨折。
Objective To evaluate the diagnostic value of X-ray in osteogenesis imperfecta of fetus.
目的评估X线对胎儿期成骨不全的诊断价值。
Methods To review the effect of intravenous pamidronate therapy on two patients with osteogenesis imperfecta in 2007.
方法对2007年我院收治的2例成骨不全症的治疗进行回顾分析。