Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy

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Coincidence of Incomplete Pentalogy of Cantrell and Meningomyelocele in a Dizygotic Twin Pregnancy

Pentalogy of Cantrell is an extremely rare and lethal syndrome. Ectopia cordis is frequently found in fetuses with POC but not required for incomplete forms. Likewise, meningomyelocele is a relatively uncommon neural tube defect affecting central nervous system and associated with neurological problems. Herein, we presented a woman with dizygotic twin pregnancy having coincidence of incomplete ...

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An incomplete pentalogy of Cantrell.

Pentalogy of Cantrell is a rare entity of congenital defects involving the abdominal wall, sternum, diaphragm, pericardium and heart. The complete pentalogy and its variants have been described in the literature. We report a 47-day-old girl with an incomplete pentalogy of Cantrell presenting with congenital absence of the sternum, congenital heart defects, and an epigastric hernia. Two even rar...

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Pentalogy of Cantrell Cantrell pentalojisi

Ectopia cordis is a rare malformation presenting as an isolated lesion or as part of the Cantrell’s pentalogy syndrome characterized by midline closure defects. A preterm male baby who did not have antenatal follow-up was born by caesarean section with evisceration of the heart and major parts of the intraabdominal organs. Combination of these findings suggested the diagnosis of Cantrell’s pent...

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Pentalogy of Cantrell

Özet İlk olarak 1958 yılında Cantrell, Haller ve Ravitch tarafından tanımlanan Cantrell sendromu, ektopia kordis ile birlikte diyafragma, orta hat karın duvarı ve perikardı etkileyen nadir görülen bir anomalidir. Cantrell sendromu sıklıkla intrakardiyak defektler ile birliktelik göstermektedir. Kompleks kardiyak anomali prognozu belirlemede önemli bir role sahiptir. Çeşitli derecelerde birçok s...

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Pentalogy of Cantrell: a case report

Cantrell's pentalogy (CP), a rare congenital malformation, consists of the supraumbilical abdominal wall defect, the sterna lower part defect and agenesis of the anterior portion of the diaphragm, an absence of the diaphragmatic part of the pericardium, and a malformation of cardia. This case report presents a female neonate, who was born at 32 weeks of conception, weighing 1300 g and was admit...

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ژورنال

عنوان ژورنال: Case Reports in Obstetrics and Gynecology

سال: 2015

ISSN: 2090-6684,2090-6692

DOI: 10.1155/2015/629561