Williamson R A, Weiner C P, Patil S, Benda J, Varner M W, Abu-Yousef M M
Obstet Gynecol. 1987 Jan;69(1):15-20.
The inability to make a definitive diagnosis in the fetus with a sonographically identified abnormality often results in parental and physician uncertainty. An antenatal chromosome evaluation could resolve this uncertainty. Forty-one fetuses with an abnormal ultrasound examination were tested for karyotypic abnormality using a variety of specimens. Nearly one-third (13 of 41) of these fetuses had various chromosome abnormalities. There were only seven survivors in this series, underscoring the often poor prognosis when a significant ultrasound defect is detected antenatally. Knowledge of the fetal chromosome constitution in the setting of an abnormal ultrasound has important epidemiologic, cost-benefit, counseling, and pregnancy management implications.
对于超声检查发现异常的胎儿,若无法做出明确诊断,常常会导致父母和医生都感到不确定。产前染色体评估可以解决这种不确定性。使用多种标本对41例超声检查异常的胎儿进行了核型异常检测。这些胎儿中近三分之一(41例中的13例)存在各种染色体异常。该系列中仅有7名幸存者,这突出了产前检测到明显超声缺陷时预后往往较差的情况。了解超声异常情况下的胎儿染色体构成,对流行病学、成本效益、咨询和妊娠管理都具有重要意义。