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机构地区:[1]湖南省常德市妇幼保健院遗传优生科,常德市产前诊断中心,415000 [2]广西壮族自治区妇幼保健院优生遗传门诊,530000 [3]湖南省长沙市妇幼保健院遗传室,410000
出 处:《中国优生与遗传杂志》2017年第8期46-47,4,共3页Chinese Journal of Birth Health & Heredity
摘 要:目的对高危孕妇行羊水细胞染色体分析,探讨产前诊断和遗传咨询中的问题。方法分析常德市产前诊断中心1122例羊水产前诊断的结果,总结染色体异常与产前诊断指征的联系。结果成功培养1122例孕妇羊水细胞染色体,发现异常核型36例,占所有标本数3.20%,多态核型49例,占所有标本数4.36%。结论对高危指征孕妇行羊水产前诊断是一项很有必要的工作。Objective:To discuss the problems in prenatal diagnosis and genetic counseling by amniotic fluid cell chromosome analysis in pregnant women at high risk. Methods:Prenatal diagnosis results of 1122 cases from the Changde Prenatal Diagnostic Center were analyzed;and the correlation between chromosomal abnormalities and indications of prenatal diagnosis was summarized. Results:1122 cases of amniotic fluid cell chromosome were successfully cultured;36 cases had abnormal karyotype,accounting for 3.20% of all specimens,while 49 cases had polymorphism karyotype,accounting for 4.36% of all specimens. Conclusion:Prenatal diagnosis of amniotic fluid is a necessary work for pregnant women with high-risk indications.
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