A birth defect in which portions of the stomach, liver, and intestines protrude through an opening in the abdominal wall.
The seventh to tenth week of fetal development
There are no non-surgical alternatives to omphalocele repair
omphalocele (protrusion of part of the intestine through the abdominal wall)
Omphalocele is a congenital condition caused by a failure of the abdominal wall to close properly during fetal development, resulting in the intestines or other abdominal organs protruding through the abdominal wall at the base of the umbilical cord. The exact cause is often unclear, but it is associated with genetic factors, maternal conditions, and certain environmental influences. Omphalocele can occur as an isolated defect or in conjunction with other congenital anomalies, such as chromosomal abnormalities.
The presence of an omphalocele often occurs with other birth defects
The omphalocele repair is a surgical procedure performed under general anesthesia
Congenital defects of the lungs, omphalocele, fetal gastroschisis, bowel obstructions, hypoplastic left heart syndrome, X-linked severe combined immunodeficiency syndrome, spina bifida.
An omphalocele is a defect that can be viewed on sonogram during an ultrasound performed while the mother is pregnant
Usually caused by a narrowing in the small intestine.
performed to repair the omphalocele defect in which all or part of the bowel and other internal organs lie on the outside of the abdomen in a hernia (sac).
An omphalocele occurs in about one in 5,000 live births
In which the blood flow through the left side of the heart is obstructed.