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...
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Format: | Article |
Language: | English |
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Wiley
2012-01-01
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Series: | Case Reports in Medicine |
Online Access: | http://dx.doi.org/10.1155/2012/428749 |
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author | Fatih Firinci Alper Soylu Belde Kasap Demir Mehmet Turkmen Salih Kavukcu |
author_facet | Fatih Firinci Alper Soylu Belde Kasap Demir Mehmet Turkmen Salih Kavukcu |
author_sort | Fatih Firinci |
collection | DOAJ |
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. |
format | Article |
id | doaj-art-35b012a89e464043a9e6e3af3a03ed09 |
institution | Kabale University |
issn | 1687-9627 1687-9635 |
language | English |
publishDate | 2012-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Medicine |
spelling | doaj-art-35b012a89e464043a9e6e3af3a03ed092025-02-03T06:01:18ZengWileyCase Reports in Medicine1687-96271687-96352012-01-01201210.1155/2012/428749428749An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with NephrolithiasisFatih Firinci0Alper Soylu1Belde Kasap Demir2Mehmet Turkmen3Salih Kavukcu4Department of Pediatrics, Dokuz Eylul University, 35340 Izmir, TurkeyDepartment of Pediatric Nephrology, Dokuz Eylul University, 35340 Izmir, TurkeyDepartment of Pediatrics, Gaziantep Education Hospital, 27560 Gaziantep, TurkeyDepartment of Pediatric Nephrology, Dokuz Eylul University, 35340 Izmir, TurkeyDepartment of Pediatric Nephrology, Dokuz Eylul University, 35340 Izmir, TurkeyPatients 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.http://dx.doi.org/10.1155/2012/428749 |
spellingShingle | Fatih Firinci Alper Soylu Belde Kasap Demir Mehmet Turkmen Salih Kavukcu An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis Case Reports in Medicine |
title | An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis |
title_full | An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis |
title_fullStr | An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis |
title_full_unstemmed | An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis |
title_short | An 11-Year-Old Child with Autosomal Dominant Polycystic Kidney Disease Who Presented with Nephrolithiasis |
title_sort | 11 year old child with autosomal dominant polycystic kidney disease who presented with nephrolithiasis |
url | http://dx.doi.org/10.1155/2012/428749 |
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