Journals / Çukurova Üniversitesi Tıp Fakültesi Dergisi / 2001 / Cilt: 26 - Sayı: 4

Prune-belly syndrome: A case report

Prune-belly sendromu: Bir olgu sunumu

Pages
185–188
Publication Date
2022-10-10
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We presented a prune-belly case with cryptorchidism, hydroureteronephrosis and atrioventricular septal defect and reviewed the literature about the etiology and treatment.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Prune-belly (Eagle-Barret) syndrome is a rare condition with deficiency of abdominal musculature, cryptorchidism and urinary tract anomalies.
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Key Findings & Data:Prune-belly (Eagle-Barret) syndrome is a rare condition with deficiency of abdominal musculature, cryptorchidism and urinary tract anomalies.
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Conclusion & Impact:We presented a prune-belly case with cryptorchidism, hydroureteronephrosis and atrioventricular septal defect and reviewed the literature about the etiology and treatment.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Prune-belly (Eagle-Barret) syndrome is a rare condition with deficiency of abdominal musculature, cryptorchidism and urinary tract anomalies. We presented a prune-belly case with cryptorchidism, hydroureteronephrosis and atrioventricular septal defect and reviewed the literature about the etiology and treatment.

Özet

Prune-belly (Eagle-Barret) sendromu, abdominal kas yokluğu, inmemiş testis ve üriner sistem anomalileri ile birlikte seyreden ve nadir görülen bir sendromdur. Burada yenidoğan yoğun bakım ünitemizde izlenen kriptorşidizm, hidroüreteronefroz ve atriyoventriküler septal defekti olan bir prune-belly sendromu olgusu sunulmuş ve literatür gözden geçirilerek etiyoloji ve tedavisi tartışılmıştır.

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Cite This Article

NARLI, N., KIRIMİ, E., SATAR, M., YAPICIOĞLU, H., SEZGİN, Y., SOYUPAK, S. (2022). Prune-belly syndrome: A case report. Çukurova Üniversitesi Tıp Fakültesi Dergisi, Cilt: 26 - Sayı: 4, 185–188. https://ajindex.com/articles/486106

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