✨
AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
This case is reportedbecause of it's rare occurence and of late diagnosis
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Xanthinuria, an inherited disorder of purine metabolism, is a rare cause of urolithiasis.
📊
Key Findings & Data:Our case presented withhematuria and crystalluria since 3 months of age.
💡
Conclusion & Impact:This case is reportedbecause of it's rare occurence and of late diagnosis
🔬Design:Article
📍Scope:Comprehensive Sample
⚙️Variables:classical xanthinuria · xanthin stone · urolitihiasis
Abstract
Xanthinuria, an inherited disorder of purine metabolism, is a rare cause of urolithiasis. Our case presented withhematuria and crystalluria since 3 months of age. He had been hospitalized for the first time at 9 months of agewith anuria and renal failure. Bilateral multiple nonopaque stones had been detected and he had undergonenephrolithotomy twice since then. He was admitted to our hospital when he was 30-months-old. He was screenedfor metabolic abnormalities and the diagnosis of classical xanthinuria was established. This case is reportedbecause of it's rare occurence and of late diagnosis
Özet
-
🔖
Cite This Article
Serdaroglu, E., Ural, R., Çalkavur, Ş., Ağın, H., Bak, M. (2003). Classical Xanthinuria: A Case Report. Meandros Medical And Dental Journal, Volume: 4 Issue: 3. https://ajindex.com/articles/1291413