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Pediatr Surg Int ; 21(6): 474-7, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15868169

RESUMEN

Congenital pouch colon (CPC), an unusual high anorectal malformation in which a varying length of colon is replaced by a dilated pouch, has appeared in a number of case reports and series published in the English literature. There is only one case report of its association with prune belly syndrome (also known as triad syndrome, Eagle-Barrett syndrome, and abdominal muscle deficiency syndrome). We report the description and management of this rare association in a male neonate with CPC, prune belly syndrome, and congenital megalourethra.


Asunto(s)
Colon/anomalías , Síndrome del Abdomen en Ciruela Pasa/complicaciones , Uretra/anomalías , Humanos , Ileostomía , Recién Nacido , Masculino , Uretra/cirugía
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