Abstract:
Prune belly syndrome (PBS) is a triad of an abdominal
wall deficiency in muscular tissue, cryptorchidism,
and dilated urinary tract. The incidence of PBS has
been reported to be 1 in 29,000 to 1 in 40,000 live
births. [1] Congenital pouch colon is a rare type of
anorectal malformation, in which the colon is malformed
into a retort‐shaped pouch partly or totally. Association
of congenial pouch colon with prune belly syndrome
is extremely rare, and there are only four such cases
reported in the English literature.
