首页> 外国专利> METHOD FOR PREDICTION OF SEVERE PREECLAMPSIA IN PREGNANT WOMEN ACCOMPANYING A MUTATION OF THE PROTHROMBIN GENE, GENOTYPE F2G20210A

METHOD FOR PREDICTION OF SEVERE PREECLAMPSIA IN PREGNANT WOMEN ACCOMPANYING A MUTATION OF THE PROTHROMBIN GENE, GENOTYPE F2G20210A

机译:F2G20210A型凝血酶原基因突变在孕妇中预测重度肥胖的方法

摘要

FIELD: medicine.;SUBSTANCE: invention relates to medicine, in particular to laboratory diagnostics, and can be used for prediction of severe preeclampsia (PE) in pregnancy in females, carriers of mutation of prothrombin gene (factor 2), genotype G20210A, by prothrombin activity detection in gestation period of 7–8 weeks. A method for predicting preeclampsia involves determining prothrombin activity by using substrate-deficient plasma, and if observing prothrombin activity 180 %, provided that 100 % corresponds to plasma 1 IU/ml prothrombin concentration, a risk of developing severe preeclampsia.;EFFECT: method enables providing more accurate prediction of developing severe preeclampsia.;1 cl, 2 dwg, 3 ex
机译:凝血酶原基因突变的载体(因子2),基因型为G20210A凝血酶原活性检测在妊娠7–8周内。一种预测先兆子痫的方法涉及通过使用底物缺陷型血浆确定凝血酶原活性,如果观察到凝血酶原活性> 180%,前提是100%对应血浆1 IU / ml凝血酶原浓度,则有发展为严重先兆子痫的风险。能够更准确地预测严重子痫前期的发展。; 1 cl,2 dwg,3 ex

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