An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular...
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doaj-96295f7a84c346b39143f932c55a664d2020-11-24T22:33:29ZengHindawi LimitedCase Reports in Nephrology2090-66412090-665X2012-01-01201210.1155/2012/978170978170An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney DiseaseFausta Catapano0Stefano Pancaldi1Carlo Pace Napoleone2Lucia Barbara De Sanctis3Gaetano Gargiulo4Giuseppe Emiliani5Antonio Santoro6Division of Nephrology, Dialysis and Hypertension, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyCardiology Unit, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyPediatric Cardiac Surgery Unit, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyDivision of Nephrology, Dialysis and Hypertension, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyPediatric Cardiac Surgery Unit, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyNephrology and Dialysis Unit, Ospedale Santa Maria delle Croci, 48121 Ravenna, ItalyDivision of Nephrology, Dialysis and Hypertension, Policlinico S. Orsola-Malpighi, 40138 Bologna, ItalyAutosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular abnormalities, are widely known manifestations. Instead intracardiac aneurysms have never been reported in adults with autosomal dominant polycystic kidney disease. We describe a 65-year-old patient with end-stage renal disease due to autosomal dominant polycystic kidney disease and an atrial septum aneurysm associated with platypnoea-orthodeoxia syndrome.http://dx.doi.org/10.1155/2012/978170 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fausta Catapano Stefano Pancaldi Carlo Pace Napoleone Lucia Barbara De Sanctis Gaetano Gargiulo Giuseppe Emiliani Antonio Santoro |
spellingShingle |
Fausta Catapano Stefano Pancaldi Carlo Pace Napoleone Lucia Barbara De Sanctis Gaetano Gargiulo Giuseppe Emiliani Antonio Santoro An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease Case Reports in Nephrology |
author_facet |
Fausta Catapano Stefano Pancaldi Carlo Pace Napoleone Lucia Barbara De Sanctis Gaetano Gargiulo Giuseppe Emiliani Antonio Santoro |
author_sort |
Fausta Catapano |
title |
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease |
title_short |
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease |
title_full |
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease |
title_fullStr |
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease |
title_full_unstemmed |
An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease |
title_sort |
unusual cardiac manifestation in autosomal dominant polycystic kidney disease |
publisher |
Hindawi Limited |
series |
Case Reports in Nephrology |
issn |
2090-6641 2090-665X |
publishDate |
2012-01-01 |
description |
Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal and extrarenal, cystic and noncystic manifestations. Connective tissue defects, including cerebral aneurysm, meningeal diverticula, abdominal wall hernias, intestinal diverticula, and cardiac valvular abnormalities, are widely known manifestations. Instead intracardiac aneurysms have never been reported in adults with autosomal dominant polycystic kidney disease. We describe a 65-year-old patient with end-stage renal disease due to autosomal dominant polycystic kidney disease and an atrial septum aneurysm associated with platypnoea-orthodeoxia syndrome. |
url |
http://dx.doi.org/10.1155/2012/978170 |
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