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VACTERL-H综合征:孕早期诊断

VACTERL-H syndrome: first trimester diagnosis.

作者信息

Dane Banu, Kayaoğlu Zeynep, Dane Cem, Aksoy Figen

机构信息

Department of Gynecology and Obstetrics, Haseki Training and Research Hospital, İstanbul, Turkey.

Department of Pathology, Cerrahpaşa Faculty of Medicine, İstanbul University, İstanbul, Turkey.

出版信息

J Turk Ger Gynecol Assoc. 2011 Dec 1;12(4):266-9. doi: 10.5152/jtgga.2011.62. eCollection 2011.

Abstract

We present two consecutive female fetuses with identical upper limb anomalies. The first of the cases was found to have ventriculomegaly, atrial septal defect, anal atresia, narrowing of the duodenal lumen and unilateral renal agenesis at the end of the second trimester. These abnormalities were characteristic of autosomal recessive VACTERL-H syndrome. The second case was diagnosed to have absent radii and thumbs at 11 weeks. Detailed examination of fetal limbs in the first trimester screening in cases with high risk is useful for early detection of this malformation.

摘要

我们报告了两名患有相同上肢异常的连续女性胎儿。第一例在孕中期末被发现有脑室扩大、房间隔缺损、肛门闭锁、十二指肠腔狭窄和单侧肾缺如。这些异常是常染色体隐性VACTERL-H综合征的特征。第二例在孕11周时被诊断为桡骨和拇指缺如。对高危病例进行孕早期筛查时对胎儿肢体进行详细检查,有助于早期发现这种畸形。

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本文引用的文献

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