ABO血型系统
胎儿
有核红细胞
基因型
黄疸
医学
产前诊断
产科
血型(非人类)
免疫学
怀孕
男科
生理学
生物
胃肠病学
遗传学
基因
作者
Lin Cheng,Xiaoyun Wei,Zixiang Wang,Chun Feng,Qing Gong,Yourong Fu,Xingzhong Zhao,Yuanzhen Zhang
标识
DOI:10.1002/elps.201900292
摘要
ABO hemolytic disease of the newborn (ABO-HDN), which may cause neonatal jaundice and polycythemia, or even stillbirth or neonatal death, is widespread in China. Prenatal testing for the fetal ABO blood group can reduce unnecessary concerns or ensure prompt treatment. Herein, we presented a method to employ high-density silica microbeads (SiO2 MBs) for capturing fetal nucleated red blood cells (fnRBCs) in maternal peripheral blood, and we detected the ABO genotype of the fetus using these captured cells. We evaluated 52 patients using the SiO2 MBs. Among 26 pregnant women with type O blood, 8 (30.8%) of the fetuses had type A blood, 5 (19.2%) had type B blood, and 13 (50%) had type O blood. SRY genes were detected in all 27 male fetuses. This study represents a simple and effective method for noninvasive prenatal detection of the fetal ABO genotype. We believe that this method has great potential for noninvasive prenatal testing of the fetal Rh blood group and other fetal diseases as well.
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