An 11-year-old child with autosomal dominant polycystic kidney disease who presented with nephrolithiasis.

Case Reports in Medicine
Fatih FirinciSalih Kavukcu

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.

References

Jun 1, 1987·Pediatric Clinics of North America·M S PolinskyH J Baluarte
Apr 1, 1988·American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation·V E TorresJ W Segura
Oct 1, 1993·American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation·V E TorresJ W Segura
Jul 20, 1999·Kidney International·N HateboerD Ravine
Jun 30, 2000·American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation·S A GrampsasP Gabow
Jan 9, 2004·The New England Journal of Medicine·Patricia D Wilson
Apr 17, 2004·Kidney International·Gordon F GibbsVicente E Torres

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Citations

Jan 13, 2018·Frontiers in Pediatrics·Stéphanie De RechterDjalila Mekahli
May 31, 2020·IUBMB Life·Mayssa AbdelwahedNeïla Belguith

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Methods Mentioned

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