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Babies who have gastroschisis typically are born at 34 to 38 weeks’ gestational age and undergo placement of a silo or primary abdominal closure within the first few hours after birth (Fig. 1). In general, affected infants do not have other life-threatening anomalies, and surgical management may be directed at repair of the intestinal herniation and abdominal wall defect. All affected infants have malrotation because the intestine failed to return to the abdominal cavity and become internally fixed. Approximately 10% have an intestinal atresia. Other anomalies are rare, in contrast to the infants who have omphalocele, in whom 50% have chromosomal with or without anatomic anomalies.

The timing and method of delivery for infants who have gastroschisis remain somewhat controversial. One of the potential complications of the condition is the development of thickened bowel or a peel that makes...

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