PRUNE BELLY SYNDROME ASSOCIATED WITH BILATERAL MULTICYSTIC DYSPLASTIC KIDNEYS AND URETHRAL OBSTRUCTION: A CASE REPORT
Arzu Akdag, Sule Arici, Betul Orhaner, Anil Dogan
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 Bellysyndrome who had abdominal muscle deficiency, multicystic dysplastic kidney,urethral hypoplasia and pulmonary hypoplasia. We presented this rare case withthe data gathered from the literature.
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