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全髋关节置换治疗终末期血友病性髋关节炎进展 被引量:6

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摘要 血友病(hemophilia)是一种X染色体连锁的出血性隐性遗传病,是凝血因子基因突变导致凝血因子Ⅷ缺乏(血友病A)或凝血因子Ⅸ缺乏(血友病B)所致。最常见的并发症是肌肉骨骼的出血,特别是在关节内的出血,常伴有关节结构的改变,称为“血友病性关节炎”(hemophilic arthropathy,HA)[1-2]。HA常累及膝、踝、肘关节,髋关节受累较少。即使髋HA的发病率较其他关节低,但因髋关节是人体主要的承重关节,其病变正逐渐受到广大医生和患者的重视[3]。
作者 李钊 陈世荣
出处 《实用骨科杂志》 2019年第8期719-723,共5页 Journal of Practical Orthopaedics
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  • 1何志勇,吴海山,狄正林,章军辉,冯建翔.全膝置换术治疗晚期血友病性膝关节炎疗效分析[J].中国骨伤,2006,19(7):395-397. 被引量:9
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  • 8Wang K, Street A, Dowrick A, et al. Clinical outcomes and patient satisfaction following total joint replacement in hae- mophilia- 23- year experience in knees, hips and elbows. Haemophilia, 2012, 18(1): 86-93.
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