[先天性X因子缺乏症,普劳瑟-斯图尔特缺乏症]。

Bilten za hematologiju i transfuziju Pub Date : 1981-01-01
P Martinić
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引用次数: 0

摘要

先天性因子- x缺陷极为罕见,通常伴有轻度出血倾向。因子- x活性的变化是单独描述的,并取决于所使用的测试,即:通过组织或血液凝血活蛋白激活因子- x,罗素毒蛇毒液,通过中和抗体或免疫沉淀。该测试取决于特定先天性缺陷血浆的可能性或使用过滤后的牛血浆。这就是为什么很难对病例进行分类并确定止血水平的最低限度。除了简要描述因子x的一些物理、化学和生化特征外,还介绍了我们实验室发现的普劳-斯图尔特因子先天性缺陷的病例,以及鉴定和确认的结果和步骤。
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[Congenital factor X deficiency, the Prower-Stuart deficiency].

The congenital deficit of factor-X is extremely rare and usually goes with mild bleeding tendency. The variations of the factor-X activities are described individually and depend on the tests used, that is: activating factor-X by tissue or blood thromboplastin, Russel's Viper Venom, by neutralisation of the antibodies or immunoprecipitation. The test depends on the possibility of the specific congenital deficient plasma or on the use of the filtered bovine plasma. That's why it is rather difficult to classify the cases and order the minimum of the hemostatic level. Besides a short description of some physical, chemical and biochemical characteristics of factor-X, present the case with congenital deficit of Prower-Stuart factor discovered in our laboratory, together with the findings and procedures in identifying and confirming it.

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Factor XII Deficiency [Disseminated intravascular coagulation]. [Cytomegalovirus transmission by fresh blood]. [Paleoserological study of human bone remains from archaeological locations in Serbia]. [20 years'activity at the Center for the Medical Care of Hemophiliacs of Serbia].
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