Fernández-Martínez F J, Galindo A, Moreno-Izquierdo A, Gómez-Rodríguez M J, Moreno-García M, Grañeras A, Barreiro E
Servicio de Genética, Hospital 12 de Octubre, Madrid, Spain.
Prenat Diagn. 2007 Jul;27(7):648-52. doi: 10.1002/pd.1746.
To establish the utility of quantitative fluorescent polymerase chain reaction (QF-PCR) in order to determine the zygosity of multiple pregnancies, as well as to define the origin of the most frequent aneuploidies in amniotic fluid samples.
We describe the case of a monochorionic (MC) diamniotic (DA) pregnancy with phenotypically discordant twins (nuchal cystic hygroma and non-immune hydrops in twin A and no anomalies in twin B). QF-PCR was performed for rapid prenatal diagnosis in uncultured amniocytes and subsequently in cultured cells. Polymorphic markers for chromosomes X, Y, 13, 18 and 21 were used for determination of zygosity as well as sex chromosome aneuploidy.
Twin A showed a Turner Syndrome (TS) mosaicism pattern by QF-PCR in uncultured amniocytes. The monozygotic origin of the pregnancy was determined. Interphase fluorescence in situ hybridization (I-FISH) in this sample showed a mosaicism X0/XY (83/17%). Cytogenetic analysis revealed a 45,X0 karyotype in twin A and a 46,XY karyotype in twin B.
QF-PCR is a reliable tool for the determination of the zygosity independently of the chorionicity and the fetal sex in case of twin pregnancy. Testing both direct and cultured cells can provide useful results for genetic counselling in chromosomal mosaicisms.
建立定量荧光聚合酶链反应(QF-PCR)的实用性,以确定多胎妊娠的合子性,并确定羊水样本中最常见非整倍体的来源。
我们描述了一例单绒毛膜(MC)双羊膜囊(DA)妊娠病例,其双胎表型不一致(双胎A有颈部囊性水瘤和非免疫性水肿,双胎B无异常)。对未培养的羊水细胞进行QF-PCR以进行快速产前诊断,随后对培养细胞进行检测。使用X、Y、13、18和21号染色体的多态性标记来确定合子性以及性染色体非整倍体。
通过对未培养羊水细胞进行QF-PCR,双胎A显示出特纳综合征(TS)嵌合模式。确定了该妊娠的单合子起源。该样本的间期荧光原位杂交(I-FISH)显示为X0/XY嵌合(83/17%)。细胞遗传学分析显示双胎A的核型为45,X0,双胎B的核型为46,XY。
对于双胎妊娠,QF-PCR是一种可靠的工具,可独立于绒毛膜性和胎儿性别来确定合子性。对直接细胞和培养细胞进行检测可为染色体嵌合的遗传咨询提供有用结果。