孤立的轻度心室肿大

M. Tomlinson, M. Treadwell, S. Bottoms
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摘要

目的:染色体异常在轻度侧脑室肿大胎儿中作为一种孤立的产前超声发现的发生率尚不清楚,并且发展为更严重的脑室肿大的速度也不确定。我们希望更好地定义核型异常的发生率和胎儿的子宫内进程与孤立的轻度心室肿大。对象与方法:回顾性分析1992年7月至1994年9月我院收治的轻度脑室肥大病例94例。46例被隔离。其中25人有遗传评价,37人有连续超声检查。我们评估了11 - 15mm心房测量的核型异常频率和子宫进展。结果:在11 - 15mm心房的胎儿中,25个核型中有3个异常(47个XXY和2个47 + 21,发生率为12% (95% CI 4.2-30.1%)。在连续扫描的37例中,5例在子宫内消退,11例保持不变,20例进展(1例超过15mm)。结论:Isolat……
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated Mild Ventriculomegaly
Objective: The incidence of abnormal chromosomes in fetuses with mild lateral ventriculomegaly as an isolated prenatal ultrasound finding is not well established, and the rate of progression to more severe ventriculomegaly is uncertain. We wished to better define both the incidence of karyotypic abnormalities and the in utero course of fetuses with isolated mild ventriculomegaly.Subjects and Methods: From July 1992 to September 1994, all cases of mild ventriculomegaly at our institution were reviewed (N = 94). Forty-six were isolated. Of these, 25 had genetic evaluation, and 37 had serial ultrasound examination. We evaluated the frequencies of karyotype abnormality and in utero progression for atrial measurements of 11–15 mm.Results: In fetuses with atria 11–15 mm, three of the 25 karyotypes were abnormal (47 XXY and two 47 + 21, giving an incidence of 12% (95% CI 4.2–30.1%). Of the 37 with serial scans, five resolved in utero, 11 remained unchanged, and 20 progressed (one beyond 15 mm).Conclusion: Isolat...
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