Quent P, Weise W, Bernoth E, Hemke G
Zentralbl Gynakol. 1977;99(23):1452-7.
138 patients were referred to us to prenatal diagnosis of genetic defects. Only in 120 patients the diagnostic procedures could also be carried out. In 75% the amniocentesis was performed to establish the amnion cell culture and in 22.5% for analysis of alphafetoprotein and for performance of fetography. In 4.2% a genetic indication for interruption was found by the prenatal diagnosis. Among the 61 terminated pregnancies a premature delivery occurred in 13.1%. The operating frequency of delivery was 16.2% and the perinatal mortality was 1.6%.
138名患者被转诊至我们处进行基因缺陷的产前诊断。只有120名患者能够进行诊断程序。75%的患者进行了羊膜穿刺术以建立羊膜细胞培养,22.5%的患者用于分析甲胎蛋白并进行胎儿造影。4.2%的患者通过产前诊断发现了终止妊娠的基因指征。在61例终止妊娠中,13.1%发生了早产。分娩手术频率为16.2%,围产期死亡率为1.6%。