Prune belly syndrome associated with bilateral multicystic dysplastic kidneys and urethral obstruction: A case report

Prune belly syndrome is a rare congenital disorder defined by a characteristic clinical triad: Abdominal muscle deficiency, severe urinary tract abnormalities, and bilateral cryptorchidism. We describe a preterm neonate of Prune Belly syndrome who had abdominal muscle deficiency, multicystic dysplas...

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Bibliographic Details
Main Authors: Arzu Akdag, Sule Arici, Betul Orhaner, Anil Dogan
Format: Article
Language:English
Published: Ped Urol Case Rep 2015-06-01
Series:Pediatric Urology Case Reports
Subjects:
Online Access:http://pediatricurologycasereports.com/ojs/index.php/pucr/article/view/79/53