An 11-year-old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis

Overview

Journal Case Rep Med

Publisher Wiley

Specialty General Medicine

Date 2012 May 9

PMID 22567016

Citations 4

Authors

Fatih Firinci

Alper Soylu

Belde Kasap Demir

Mehmet Turkmen

Salih Kavukcu

Affiliations

Soon will be listed here.

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.

Citing Articles

Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience.

Demir B, Mutlubas F, Soyaltin E, Alparslan C, Arya M, Alaygut D Turk J Med Sci. 2020; 51(2):772-777.

PMID: 33315352 PMC: 8203125. DOI: 10.3906/sag-2009-79.

ADPedKD: A Global Online Platform on the Management of Children With ADPKD.

De Rechter S, Bockenhauer D, Guay-Woodford L, Liu I, Mallett A, Soliman N Kidney Int Rep. 2019; 4(9):1271-1284.

PMID: 31517146 PMC: 6732756. DOI: 10.1016/j.ekir.2019.05.015.

Is Autosomal Dominant Polycystic Kidney Disease Becoming a Pediatric Disorder?.

De Rechter S, Breysem L, Mekahli D Front Pediatr. 2018; 5:272.

PMID: 29326910 PMC: 5742347. DOI: 10.3389/fped.2017.00272.

Percutaneous Nephrolithotomy in Autosomal Dominant Polycystic Kidney Disease: Is it Different from Percutaneous Nephrolithotomy in Normal Kidney?.

Singh V, Sinha R, Gupta D Curr Urol. 2014; 7(1):7-13.

PMID: 24917749 PMC: 3783285. DOI: 10.1159/000343545.

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