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唐氏综合征胎儿的脐静脉异常。

Umbilical vein anomaly in fetuses with Down syndrome.

机构信息

Department of Obstetrics and Gynecology, The Chaim Sheba Medical Center, Tel Hashomer, affiliated with the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Ultrasound Obstet Gynecol. 2010 Mar;35(3):297-301. doi: 10.1002/uog.7542.

Abstract

OBJECTIVE

To describe the prevalence of abnormal umbilical vein (UV) anatomy in fetuses with Down syndrome.

METHODS

This was a retrospective survey covering a 24-month period of fetuses with a genetic diagnosis of Down syndrome following a routine early second-trimester (12-16-week) detailed fetal anomaly scan at a single academic tertiary referral center. In our unit this exam includes fetal umbilicoportal venous system evaluation.

RESULTS

During the study period, 37 fetuses were diagnosed with Down syndrome and had a detailed early anatomy scan. In four (11%) the detailed early anomaly scan revealed that the UV was connected to the hepatic portion of the inferior vena cava (IVC) at a position lower than its usual site. Their average gestational age at diagnosis was 13 + 6 (range, 11 + 6 to 15 + 2) weeks. Three of the four fetuses had a nuchal translucency thickness of 3-4 mm. In one fetus there was an additional finding of significant tricuspid regurgitation and the one with normal nuchal translucency thickness had an atrioventricular septal defect (atrioventricular canal) and umbilical cord hernia. During the same period three of 2500 (0.12%) fetuses with normal karyotype demonstrated similar anomalous insertion of the UV into the IVC, creating a portocaval shunt which had normal ductus venosus-like Doppler flow in all three cases. The odds ratio for abnormal umbilicoportal venous system in fetuses with Down syndrome compared with the normal population was 107.4 (95% CI, 19.2-637.1).

CONCLUSIONS

Fetuses with Down syndrome demonstrate an increased prevalence of abnormal connection of the UV to the IVC.

摘要

目的

描述唐氏综合征胎儿脐静脉(UV)解剖结构异常的发生率。

方法

这是一项回顾性调查,涵盖了在单一学术三级转诊中心进行常规孕中期(12-16 周)详细胎儿异常扫描后,对唐氏综合征进行遗传诊断的 24 个月期间的胎儿。在我们的单位,该检查包括胎儿脐门静脉系统评估。

结果

在研究期间,37 例胎儿被诊断为唐氏综合征,并进行了详细的早期解剖扫描。在 4 例(11%)中,详细的早期异常扫描显示,UV 在低于其通常位置与下腔静脉(IVC)的肝段相连。他们的平均诊断孕周为 13+6(范围 11+6 至 15+2)周。4 例中有 3 例颈后透明带厚度为 3-4 毫米。其中 1 例胎儿还存在严重的三尖瓣反流,而颈后透明带厚度正常的胎儿存在房室间隔缺损(房室管)和脐带疝。在此期间,在 2500 例正常核型胎儿中,有 3 例(0.12%)出现类似的脐静脉异常插入 IVC,形成门腔分流,所有 3 例均存在正常的静脉导管样多普勒血流。唐氏综合征胎儿脐门静脉系统异常的比值比为 107.4(95%CI,19.2-637.1)。

结论

唐氏综合征胎儿脐静脉与 IVC 的异常连接发生率增加。

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