Complete duplication of the urinary bladder: An extremely rare congenital anomaly

膀胱完全重复畸形:一种极其罕见的先天性异常

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Abstract

A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis. The patient underwent several investigations and undergoing multistage surgical intervention.

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