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。
A novel collagen, type ⅰ, alpha ⅰ mutation in a Chinese osteogenesis imperfecta family Significance of PTEN and PCNA's expression in human glioma 成骨不全(OI)一家系1型胶原α1链基因新突变PTEN基因和增殖细胞核抗原在原发胶质瘤中的表达及意义
Methods To review the effect of intravenous pamidronate therapy on two patients with osteogenesis imperfecta in2007. 方法对2007年我院收治的2例成骨不全(OI)症的治疗进行回顾分析。
Objective To summarize the experience of pamidronate for osteogenesis imperfecta. 目的总结帕米膦酸钠在成骨不全(OI)症中的应用经验。
Methods : The clinical radiographic and CT features of 6 patients with tumoral callus of 68 osteogenesis imperfecta were analysed retrospectively. 方法:对一组68例成骨不全(OI)中6例并有肿瘤样骨痂的临床、X线和CT表现进行回顾性分析。