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NDT Advance Access originally published online on October 24, 2006
Nephrology Dialysis Transplantation 2007 22(2):652-653; doi:10.1093/ndt/gfl615
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© The Author [2006]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
(Section Editor: G. H. Neild)

Polycystic horseshoe kidney

Luis Alberto Batista Peres1, José Roberto Leonel Ferreira2 and Vinicius Daher Alvares Delfino3

1Department of Nephrology, 2Department of Radiology, State University of West of Paraná and 3Nephrology Department, State University of Londrina, Brazil

Correspondence and offprint requests to: Luis Alberto Batista Peres. Email: vddelfino@sercomtel.com.br

Keywords: horseshoe; kidney disease; polycystic

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Introduction

Polycystic horseshoe kidney is thought to represent two separate renal diseases. Horseshoe kidney is a renal fusion anomaly during embryogenesis; autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder due to mutations in the genes responsible for the expression of the . . . [Full Text of this Article]

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A. Connor, C. E. Weston, C. Dick, and J. E. Taylor
Autosomal dominant polycystic kidney disease complicating renal ectopia and managed with renal transplantation
NDT Plus, October 1, 2009; 2(5): 420 - 420.
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