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凝血因子X缺乏症是一种罕见的常染色体隐性遗传病。根据近代研究证明:因子X不但是组织凝血活素系统(亦称外在凝血活素系统)的组成部分之二一,也是血液凝血活素系统(亦称内在凝血活素系统)不可缺少的一部份。因此,Macfarlane等对因子X在凝血活酶形成中的地位估价中提出:因子X的激活是各种凝血活酶形成的中心环节。①因子X一但缺乏,凝血活
Factor X deficiency is a rare autosomal recessive disease. According to modern studies, Factor X is not only one of the components of the thromboplastin system (also known as the external thromboplastin system), but also an integral part of the hemagglutinin system (also known as the intrinsic thromboplastin system) Part Therefore, Macfarlane and other factor X in the formation of thromboplastin position evaluation put forward: the activation of factor X is the central part of the formation of various thromboplastin. ① factor X, but lack of clotting activity