Complete Duplication of the Male Urethra

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First Case of Complete Bladder Duplication in the Coronal Plane with Concomitant Duplication of the Urethra in an Adult Male

Duplication of the lower urinary tract is a very rare congenital anomaly which is diagnosed either at birth or during early childhood. These rare malformations are most of the times accompanied by other concomitant anomalies and are therefore diagnosed immediately after birth. In some even rarer cases there are no concomitant anomalies and symptoms thus leading to a diagnosis later in childhood...

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Complete duplication of urinary bladder and urethra: prenatal sonographic features.

Prenatal sonographic features of the rare anomaly of complete duplication of the urinary bladder and urethra are described in this case report. A coronal scan of the fetal pelvis at 29 weeks of gestation revealed two pyriform cystic structures. The umbilical arteries coursed around both of them. They emptied independently of each other. Postnatally the newborn had two vulvae, two anal openings,...

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Complete duplication of bladder and urethra: a case report.

A case of complete duplication of the bladder and urethra in a girl is reported, demonstrating outlet obstruction in the bladder on the left side. Associated anomalies and pertinent literature are reviewed.

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Complete colonic duplication in children

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Diseases of the Male Urethra

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ژورنال

عنوان ژورنال: Annals of Surgery

سال: 1957

ISSN: 0003-4932

DOI: 10.1097/00000658-195701000-00014