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妊娠12周时伴有脊柱侧弯和马蹄内翻足畸形的坎特雷尔五联症。

Pentalogy of Cantrell accompanied by scoliosis and pes equinovarus deformity at 12 weeks gestation.

作者信息

Pekin A Tazegül, Kerimoğlu O Seçilmiş, Yilmaz S A, Kebapcilar A G, Bakbak B Gencoğlu, Celik C

出版信息

Clin Exp Obstet Gynecol. 2015;42(3):392-4.

Abstract

Cantrell's pentalogy (CP) is a rare syndrome characterized by defects in the lower sternum with ectopia cordis, anterior diaphragm defects, midline supraumbilical abdominal wall defects, defects in the diaphragmatic pericardium, and congenital heart disease. The authors report a 12-weeks gestation with multiple fetal anomalies suggesting the diagnosis of CP (a large thoraco-abdominal defect with herniating liver and bowel, heart deviated anteriorly with concomitant ventricular septal defect), and the 'S' shaped fetal spine due to increased lumbar lordosis and scoliosis with accompanying pes equinovarus deformity. Chorionic villus sampling was performed due to increased nuchal translucency (3.7 mm). The fetal karotype was found to be 47, XX,+21 (trisomy 21). In the literature, three scoliosis cases have been reported accompanying the CP along with multiple anomalies and one concomitant pes equinovarus deformity has been reported previously.

摘要

坎特雷尔五联症(CP)是一种罕见综合征,其特征为下胸骨缺损合并心脏异位、前膈缺损、脐上中线腹壁缺损、膈心包缺损以及先天性心脏病。作者报告了一例妊娠12周的孕妇,胎儿存在多种异常,提示CP诊断(巨大胸腹缺损伴肝脏和肠管疝出、心脏向前移位并伴有室间隔缺损),且胎儿脊柱呈“S”形,原因是腰椎前凸增加和脊柱侧弯,并伴有马蹄内翻足畸形。由于颈项透明层增厚(3.7毫米),进行了绒毛取样。胎儿核型为47, XX, +21(21三体综合征)。文献中曾报告过3例CP合并脊柱侧弯及多种异常的病例,此前也曾报告过1例合并马蹄内翻足畸形的病例。

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