Martinić P
Bilt Hematol Transfuz. 1979;7(2-3):151-8.
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.
在发表于《血液学与输血学通报》上的上一篇论文中,我们描述了哈格曼因子(HF)先天性缺乏症及基本研究结果。现在,我们提供更多实验室诊断测试,以明确证实我们的患者缺乏凝血因子 XII,而非接触凝血阶段的其他一些因子,如弗莱彻因子、菲茨杰拉德因子、威廉姆斯因子和弗洛热阿克因子。另一方面,为了阐明在解决这些病例时可能面临的实验室诊断问题,我们回顾了接触因子的基本生化特性以及内源性凝血途径启动机制。