Abstract
Congenital obstruction of intestine is a rare genetic disorder with the incidence 1:3000-5000 live-born infants. The detection can be antenatal using ultrasound examination.
The picture of dilated intestinal loops or polyhydramnia is a typical finding. Prenatal diagnostics of acute intestinal perforation is very difficult.
In English literature, there is only a case report of inborn intestine perforation in foetus with gastroschisis. Only a few cases of intestinal atresia are reported that were recognized in prenatal period.
The following perforation of gut was diagnosed after the birth.