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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
This case is discussed in terms of the type of urethral duplication and the importance of additional anomalies.
📌 3 Key Takeaways
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Objective & Hypothesis:Urethral duplication is a rare congenital malformation with multiple clinical manifestations.
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Key Findings & Data:Here, we present a case involving a boy with hypospadiac urethral duplication and multiple congenital anomalies.
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Conclusion & Impact:This case is discussed in terms of the type of urethral duplication and the importance of additional anomalies.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Özet
Urethral duplication is a rare congenital malformation with multiple clinical manifestations. Here, we present a case involving a boy with hypospadiac urethral duplication and multiple congenital anomalies. The patient had additional anomalies including a posterior urethral valve, left vesicoureteral reflux and right renal agenesis. This case is discussed in terms of the type of urethral duplication and the importance of additional anomalies.
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Cite This Article
BASUGUY, E., BAYRAM, S. (2019). A rare case with multiple urinary anomalies associated with urethral duplication: Distal hypospadias, posterior urethral valve, left vesicoureteral reflux, and right renal agenesis. Pediatric Urology Case Reports, Cilt: 6 - Sayı: 1, 1–4. https://ajindex.com/articles/285544