Abstract

• Gastroshisis is a rare congenital defect demanding urgent surgical correction. It is a full thickness cleft of the abdominal wall next to the insertion of the cord through which the intestines are eviserated. The characteristics which differentiate gastroschisis from omphalocele are the extra-umbilical location of the abdominal wall defect, the normal insertion of the umbilical cord, and the abscence of a covering sac or its ruptured remnants.
  The child had unevenful postoperative course and has grow up normal and healthy. This paper is concerned with our experience of a survival case and reviewed the embryo-logy, pathology, associated anormalities, and the current concepts in the management of gastroschisis in the literatures.