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Quantitation of fetal DNA in maternal serum in normal and aneuploid prenancies.

机译:正常和整倍体妊娠孕妇血清中胎儿DNA的定量。

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We investigated whether the amount of circulating cell-free fetal DNA in maternal serum is influenced by fetal karyotype, using real-time quantitative polymerase chain reaction assay. Serum samples were obtained from pregnant women at gestational ages ranging from 15 to 17 weeks, prior to their undergoing amniocentesis. In total, we examined 70 samples consisting of 55 cases of pregnancy with 46,XY, 5 cases with 47,XY,+21, 3 cases with 47,XY,+18, a single case with 46,XY,dup(1) and 2 cases with twins of 46,XY, and 4 cases with 46,XX which were used as negative controls. We measured the concentration of the SRY sequence as a molecular marker for fetal DNA. The SRY sequence was detectable and measurable when the fetuses were male except for one case with 47,XY,+18. This case showed fetal growth retardation and bradycardia. No amplification signals of the SRY sequence were detected when the fetuses were female. The mean concentration of fetal DNA in maternal serum was 31.5 copies/ml in the pregnancy with 46,XY, 23.5 copies/ml in the pregnancies with 47,XY,+21 and 21.5 copies/ml in the pregnancies with 46,XY,+18. There were no significant differences in the concentration of fetal DNA between pregnancies with fetuses of normal karyotype and those with fetuses of abnormal karyotype.
机译:我们使用实时定量聚合酶链反应测定法调查了母体血清中循环的无细胞胎儿DNA的量是否受胎儿核型的影响。在孕妇进行羊膜穿刺术之前,从15至17周的胎龄孕妇中获取血清样本。我们总共检查了70个样本,其中包括55个怀孕的46,XY例,5个47,XY,+ 21例,3个47,XY,+ 18例,一个46,XY,dup例(1) 2例46,XY双胞胎和4例46,XX双胞胎用作阴性对照。我们测量了SRY序列的浓度,作为胎儿DNA的分子标记。胎儿为男性时,SRY序列是可检测和可测的,只有47,XY,+ 18的情况除外。该病例显示胎儿发育迟缓和心动过缓。当胎儿是雌性时,未检测到SRY序列的扩增信号。孕妇血清中胎儿DNA的平均浓度在妊娠为46,XY的孕妇中为31.5拷贝/ ml,在妊娠为47,XY,+ 21的孕妇中为23.5拷贝/ ml,在妊娠为46,XY,+的孕妇中为21.5拷贝/ ml。 18岁正常核型胎儿和异常核型胎儿的胎儿DNA浓度没有显着差异。

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