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Updated: May 22, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
An 11-year-old child with autosomal dominant polycystic kidney disease who presented with nephrolithiasis
Fatih Firinci1, Alper Soylu, Belde Kasap Demir
1Department of Pediatrics, Dokuz Eylul University, 35340 Izmir, Turkey.
Abstract:
Patients with autosomal dominant polycystic kidney disease become symptomatic and are diagnosed usually at adulthood. The rate of nephrolithiasis in these patients is 5-10 times the rate in the general population, and both anatomic and metabolic abnormalities play role in the formation of renal stones. However, nephrolithiasis is rare in childhood age group. In this paper, an 11-year-old child with autosomal dominant polycystic kidney disease presenting with nephrolithiasis is discussed.
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