A new variant of urethral duplication- collateral urethral duplication with paraspadiac meatus: A case report

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Novel Presentation of Complete Coronal Urethral Duplication: a Case Report

     Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astoundin...

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Collateral urethral duplication in an adult.

OBJECTIVE Congenital anomalies or malformations of the urethra that involve number are extremely rare and only 7 cases of trifurcation of the urethra and under 500 cases of urethral duplication have been described. METHODS In the case we present, urethral duplication was diagnosed in adulthood, even though glans malformation with 2 urethral orifices was clearly evident and only 1 was function...

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Urethral duplication.

Urethral duplication is a rare congenital anomaly. Although a number of theories have been proposed to describe the embryology of the condition, the actual mechanism of the disorder is still unclear. We report here a case of urethral duplication in a 11-year-old boy complaining of a double stream, and review the current literature on this rare entity.

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Complete Urethral Duplication in Children: A Case Report

INTRODUCTION Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants. CASE PRESENTATION In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD. CONCLUSIONS After one year...

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ژورنال

عنوان ژورنال: Pediatric Urology Case Reports

سال: 2018

ISSN: 2148-2969

DOI: 10.14534/j-pucr.2018133804