Domján G, Petö I, Pál A, Blaskó G, Sas G
Orv Hetil. 1989 Sep 17;130(38):2023-5.
In recent years there have been discovered more and more such connatal mostly hereditary coagulopathies, which can explain the thrombosis susceptibility of the given individual or/and the family. The International Thrombosis and Haemostasis Society made a survey to estimate the frequency of those defects causing thrombophilias. In this survey the authors analysed the cases of their patients according to the given points of view. In their work they discuss some theoretical and practical problems of the theme, which can have an importance in respect to the everyday medical practice.
近年来,人们发现了越来越多这样的先天性(大多为遗传性)凝血障碍疾病,它们能够解释特定个体或/和家族的血栓形成易感性。国际血栓与止血学会进行了一项调查,以估算导致血栓形成倾向的这些缺陷的发生率。在这项调查中,作者们根据特定的观点对他们患者的病例进行了分析。在他们的工作中,他们讨论了该主题的一些理论和实际问题,这些问题对于日常医疗实践可能具有重要意义。