Rezai K, Holzgreve W, Schloo R, Tercanli S, Horst J, Miny P
Zentrum für Frauenheilkunde, Westfälischen Wilhelms-Universität Münster.
Geburtshilfe Frauenheilkd. 1991 Mar;51(3):211-6. doi: 10.1055/s-2007-1023706.
A retrospective evaluation of 463 prenatal chromosome analyses in a total of 375 patients with suspicious ultrasound findings, revealed a high rate of severe chromosomal abnormalities (16%). The highest risk for an abnormal karyotype was found after sonographic detection of hygroma colli. Abnormal chromosome counts were also frequently found in fetuses with omphaloceles, duodenal atresia and hydrops fetalis, as well as in presence of intrauterine growth retardation and/or anomalies of the amniotic fluid volume. The anomalies mentioned above are, therefore, an urgent indication for a prenatal chromosome analysis. The technical improvements of ultrasound machines and growing experience of operators will lead to an increasing importance of sonography as a method for the identification of pregnancies, that are at high risk for chromosomal abnormalities.
对375例超声检查结果可疑的患者进行的463次产前染色体分析的回顾性评估显示,严重染色体异常的发生率很高(16%)。在超声检测到颈部水囊瘤后,发现核型异常的风险最高。在患有脐膨出、十二指肠闭锁和胎儿水肿的胎儿中,以及存在宫内生长受限和/或羊水过少的情况下,也经常发现染色体数目异常。因此,上述异常是产前染色体分析的紧急指征。超声设备的技术改进和操作人员经验的增加,将使超声检查作为一种识别染色体异常高风险妊娠的方法变得越来越重要。