## Abstract Trisomy 18 is the secondβmost common autosomal trisomy and represents one third of the chromosomal trisomies identified prenatally. We present a case of a fetus with trisomy 18 in which thoracoabdominal ectopia cordis was detected prenatally; it was noted as a dominant defect on a sonog
Complete ectopia cordis with anencephaly: A case report
β Scribed by Seema Chopra; Arun Kalpdev; Vanita Suri; Neelam Aggarwal; Meenakshi Rohilla
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 162 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0091-2751
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
We report a case of pentalogy of Cantrell with anencephaly diagnosed in utero on 2βdimensional sonography at 17 weeks of gestation. Due to associated anencephaly, termination of pregnancy was carried out. Histopathological examination confirmed the sonographic findings. Β© 2010 Wiley Periodicals, Inc. J Clin Ultrasound, 2010
π SIMILAR VOLUMES
## Abstract Ectopia cordis and mosaic trisomy 16 are two rare fetal anomalies, which have not been reported in association. We report a case of an isolated ectopia cordis at 11^+3^ weeks. Subsequent embryological examination confirmed thoracic ectopia cordis with normal heart structure and array co
This report presents the renal venous architecture in a case of a duplex kidney with crossed fused ectopia. The renal venous anatomy as defined by venography and resin cast preparation is described. The intrarenal venous flow pattern was demonstrated to be non-lobar and non-segmental. Renal vein val
## Abstract ## Background. Only 1 case with dual thyroid ectopy and a normally located thyroid gland has been reported. ## Methods. We present the case of a 71βyearβold woman who had 1βsided lateral neck swelling in the right submandibular space, which grew and doubled in size within 1 year. A C