“…Congenital duodenal obstruction accounts for half of congenital bowel obstructions [1,2], with an incidence of 1 in 5,000 to 1 in 10,000 live births [3,4]. Complicating the management of patients with congenital duodenal obstruction is the fact that nearly half of these patients are premature [1,5] and greater than half are born with other major congenital anomalies, including cardiac defects, renal anomalies, esophageal atresia/tracheoesophageal fistula, biliary anomalies and trisomy 21 [1,[5][6][7][8][9][10].…”