因子十二缺乏-哈格曼性状。附加诊断程序]。

Bilten za hematologiju i transfuziju Pub Date : 1979-01-01
P Martinić
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引用次数: 0

摘要

在之前发表在《血液学与输血公报》上的论文中,我们描述了先天性哈格曼因子(HF)缺陷的基本发现。现在我们提供额外的实验室诊断测试,以明确确认我们的患者有因子XII的缺陷,而不是其他一些接触凝血期的因素:Fletcher, Fitzgerald, Williams和Flaujeac。另一方面,为了启发在解决这些病例时可能面临的实验室诊断问题,我们对接触因子的基本生化特征和血液凝固内部途径开始的机制进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Factor XII deficiency - Hageman trait. Additional diagnostic procedures].

In the previous paper published in the Bulletin for Hematology and Blood Transfusion we described the congenital deficit of Hageman factor (HF) with the basic findings. Now we provide addilioval laboratory -diagnostical tests in order to confirm definitively that our patients have the deficit of Factor XII, and not of some other factors of the contact coagulation phase as: Fletcher, Fitzgerald, Williams and Flaujeac. On the other hand, in order to enlight the laboratory-diagnostical problems which one can face in solving of these cases, we have reviewed the basic biochemical characteristics of the contact factors and the mechanism of the beginning of the internal pathway of blood coagulation.

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