In this article a prenatally diagnosed case of pentalogy of Cantrell is presented and discussed with the review of the literature.
📌 3 Key Takeaways
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Objective & Hypothesis:Pentalogy of Cantrell is a rare congenital syndrome; characterized by partial or complete ectopia cordis, omphalocele, congenital heart defects and defects in the lower sternum, pericardium, and anterior diaphragm.
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Key Findings & Data:Pentalogy of Cantrell is a rare congenital syndrome; characterized by partial or complete ectopia cordis, omphalocele, congenital heart defects and defects in the lower sternum, pericardium, and anterior diaphragm.
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Conclusion & Impact:In this article a prenatally diagnosed case of pentalogy of Cantrell is presented and discussed with the review of the literature.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Cantrell · pentaloji · ektopia kordis
Abstract
Pentalogy of Cantrell is a rare congenital syndrome; characterized by partial or complete ectopia cordis, omphalocele, congenital heart defects and defects in the lower sternum, pericardium, and anterior diaphragm. In this article a prenatally diagnosed case of pentalogy of Cantrell is presented and discussed with the review of the literature.
Özet
Cantrell pentalojisi oldukça nadir görülen ve ektopia kordisin tam veya parsiyel formu ile birlikte omfalosel, konjenital kalp hastalıkları ve perikardiyumda, sternum alt kesiminde ve anterior diyaframda defektler ile karakterize bir sendromdur. Bu yazıda prenatal olarak tanımlanmış Cantrell sendromlu bir olgu sunularak, Cantrell sendromunun literatür eşliğinde tartışılması amaçlanmıştır.
KÜÇÜK, M., DEMİRCAN, S. S., YÜKSEL, H., ODABAŞI, A. R. (2010). A prenatally diagnosed pentalogy of Cantrell case. Pamukkale Tıp Dergisi, Cilt: 3 - Sayı: 3, 161–163. https://ajindex.com/articles/286371