Abstract
Cantrell’s pentalogy is a rare congenital malformation which consists of the supraumbilical abdominal wall defect, the defect in the lower sternum, the agenesis of the anterior portion of the diaphragm, the absence of the diaphragmatic part of the pericardium, and the structural cardiac anomaly. This congenital malformation has a high mortality rate of in the postnatal period. Its etiopathogenesis is not yet certain. It is thought to be due to the lack or inadequacy of the migration of lateral mesoderm in the early weeks of pregnancy. Five main phenotypic findings of Cantrell’s pentalogy may not always be present in the affected cases because of the alterations in the migration defects. The subjects diagnosed with Cantrell’s pentalogy can be examined in three categories based on the phenotypic features. This is a case report of a 13-week-old pregnancy which is diagnosed with Cantrell’s pentalogy due to the presence of cystic hygroma, ectopia cordis, omphalocele and atrioventricular septal defect.
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