Sherlock J, Halder A, Tutschek B, Delhanty J, Rodeck C, Adinolfi M
Department of Genetics and Biometry, Galton Laboratory, University College London, UK.
J Med Genet. 1997 Apr;34(4):302-5. doi: 10.1136/jmg.34.4.302.
In the course of an investigation aimed at detecting the presence of trophoblastic cells in the endocervical canal of pregnant women between 7 and 17 weeks of gestation, several cases of aneuploidies were observed using a fluorescent in situ hybridisation (FISH) assay. The cases include fetal chromosome 21 and 18 trisomies, triploidy and sex chromosome aneuploidies. The results were confirmed by testing placental tissues obtained after termination of pregnancy (TOP). In two of these cases, clumps of cells with the morphology of trophoblasts were isolated from the transcervical cell (TCC) samples using micromanipulation. FISH and fluorescent polymerase chain reactions (PCR), performed on these clumps, showed them to be exclusively of fetal origin. These results show that prenatal diagnoses of major aneuploidies can be performed by FISH using whole TCC samples, or on isolated clumps of cells by FISH and PCR assays.
在一项旨在检测妊娠7至17周孕妇宫颈管中滋养层细胞的调查过程中,使用荧光原位杂交(FISH)检测法观察到了几例非整倍体病例。这些病例包括胎儿21号和18号染色体三体、三倍体以及性染色体非整倍体。通过检测终止妊娠(TOP)后获得的胎盘组织证实了结果。在其中两例中,使用显微操作从经宫颈细胞(TCC)样本中分离出具有滋养层细胞形态的细胞团。对这些细胞团进行FISH和荧光聚合酶链反应(PCR)检测,结果表明它们完全来自胎儿。这些结果表明,可通过对整个TCC样本进行FISH,或通过FISH和PCR检测法对分离出的细胞团进行检测,来进行主要非整倍体的产前诊断。