Prune belly syndrome with congenital pouch colon

Annigeri, Venkatesh M.; Bhat, Manjunath T.; Hegde, Harihar V.; Annigeri, Rashmi V.; Halgeri, Anil B.

dc.contributor.author	Annigeri, Venkatesh M.
dc.contributor.author	Bhat, Manjunath T.
dc.contributor.author	Hegde, Harihar V.
dc.contributor.author	Annigeri, Rashmi V.
dc.contributor.author	Halgeri, Anil B.
dc.date.accessioned	2013-12-29T23:48:38Z
dc.date.available	2013-12-29T23:48:38Z
dc.date.issued	2013-04
dc.identifier.citation	Journal of Indian Association of Pediatric Surgeons. 2013 Apr-Jun; 18(2): 79-80.	en_US
dc.identifier.issn	0971-9261
dc.identifier.uri	http://hdl.handle.net/123456789/445
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Wolters Kluwer-Medknow	en_US
dc.subject	Congenital pouch colon	en_US
dc.subject	Hydronephrosis	en_US
dc.subject	Prune belly syndrome	en_US
dc.title	Prune belly syndrome with congenital pouch colon	en_US
dc.type	Article	en_US