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An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis

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 ston... Full description

Journal Title: Case Reports in Medicine 2012, Vol.2012, 3 pages
Main Author: Firinci, Fatih
Other Authors: Soylu, Alper , Kasap Demir, Belde , Turkmen, Mehmet , Kavukcu, Salih
Format: Electronic Article Electronic Article
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ID: ISSN: 1687-9627 ; E-ISSN: 1687-9635 ; DOI: 10.1155/2012/428749
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recordid: hindawi10.1155/2012/428749
title: An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis
format: Article
creator:
  • Firinci, Fatih
  • Soylu, Alper
  • Kasap Demir, Belde
  • Turkmen, Mehmet
  • Kavukcu, Salih
subjects:
  • Case Report
ispartof: Case Reports in Medicine, 2012, Vol.2012, 3 pages
description: 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.
language:
source:
identifier: ISSN: 1687-9627 ; E-ISSN: 1687-9635 ; DOI: 10.1155/2012/428749
fulltext: fulltext
issn:
  • 1687-9627
  • 16879627
  • 1687-9635
  • 16879635
url: Link


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titleAn 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis
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descriptionPatients 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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titleAn 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis
descriptionPatients 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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titleAn 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis
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abstractPatients 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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