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[45,X/46,XX嵌合体不一致的单绒毛膜双羊膜囊双胎的产前诊断]

[Prenatal diagnosis of monochorionic-diamniotic twins discordant for 45,X/46,XX mosaicism].

作者信息

Hu Jiancheng, Xi Hui, Ma Na, Pang Jialun, Luo Yingchun, Jia Zhengjun, Wang Hua

机构信息

Department of Medical Genetics, Maternal and Child Health Care Hospital of Hunan Province, Changsha, Hunan 410008, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):260-262. doi: 10.3760/cma.j.issn.1003-9406.2019.03.017.

Abstract

OBJECTIVE

To explore the prenatal screening and diagnosis for a pair of monochorionic-diamniotic (MCDA) twins discordant for 45,X/46,XX mosaicism.

METHODS

Amniotic fluid samples were taken from both twins for whom non-invasive prenatal testing has signaled a high risk for sex chromosomal abnormality. Uncultured amniotic fluid was analyzed by fluorescence in situ hybridization (FISH) and single nucleotide polymorphism array (SNP-array). Conventional G-banded karyotyping analysis was performed on the cultured amniotic fluid.

RESULTS

Metaphase chromosome analysis showed that one of the twins had a mos 45,X[11]/46,XX[26] karyotype, while the other had a normal karyotype. FISH and SNP-array applied on uncultured amniotic fluid revealed about 30% mosaicism in one of the twins. The twins were confirmed to be monozygotic by SNP-array analysis.

CONCLUSION

To avoid confusion arising from discordant karyotypes in MCDA twins with abnormal non-invasive prenatal testing (NIPT) results, dual amniocentesis should be carried out to obtain amniotic fluid samples for chromosomal as well as molecular analysis. To determine the ratio of 45,X and 46,XX cells in Turner syndrome can provide valuable information for prenatal genetic counseling.

摘要

目的

探讨对一对单绒毛膜双羊膜囊(MCDA)双胎进行产前筛查和诊断的方法,这对双胎存在45,X/46,XX嵌合体不一致的情况。

方法

对无创产前检测提示性染色体异常高风险的双胎均采集羊水样本。未培养的羊水通过荧光原位杂交(FISH)和单核苷酸多态性阵列(SNP-阵列)进行分析。对培养后的羊水进行常规G显带核型分析。

结果

中期染色体分析显示,其中一个双胎的核型为mos 45,X[11]/46,XX[26],而另一个双胎核型正常。对未培养羊水应用FISH和SNP-阵列检测发现其中一个双胎存在约30%的嵌合体。通过SNP-阵列分析证实这对双胎为单卵双胎。

结论

为避免无创产前检测(NIPT)结果异常的MCDA双胎核型不一致所导致的混淆,应进行双羊膜腔穿刺以获取羊水样本进行染色体及分子分析。确定特纳综合征中45,X和46,XX细胞的比例可为产前遗传咨询提供有价值的信息。

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