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Journals / Pediatric Urology Case Reports / 2015 / Cilt: 2 - Sayı: 1

Type II A2 duplication of urethra in an 8-month-old male child: A case report

MEHMET HANİFİ OKUR
BAHATTİN AYDOĞDU
SERKAN ARSLAN
EROL BASUGUY
HİKMET ZEYTUN
Mehmet Şerif ARSLAN
Pages
19–24
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

The accessory ventral urethra was excised without complication

📌 3 Key Takeaways

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Objective & Hypothesis:Urethral duplication is a rare congenital anomaly, usually found with multiple anatomical variants.
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Key Findings & Data:In this article was presented a case of urethral duplication in an 8-month-old male child.
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Conclusion & Impact:The accessory ventral urethra was excised without complication
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Urethral duplication is a rare congenital anomaly, usually found with multiple anatomical variants. In this article was presented a case of urethral duplication in an 8-month-old male child. The malformation was characterized by the presence of continent hypospadic and normal apical urethra. Retrograde urethrogram through both urethral tracts simultaneously revealed the malformation as Effmann Type II A-2. The accessory ventral urethra was excised without complication

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Cite This Article

OKUR, M. H., AYDOĞDU, B., ARSLAN, S., BASUGUY, E., ZEYTUN, H., ARSLAN, M. Ş. (2015). Type II A2 duplication of urethra in an 8-month-old male child: A case report. Pediatric Urology Case Reports, Cilt: 2 - Sayı: 1, 19–24. https://ajindex.com/articles/285706

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