Cargando…
Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is responsible for 8–10% of patients with end-stage renal failure. The major extrarenal complications of ADPKD are cardiovascular abnormalities. Interrupted aortic arch (IAA) is a lethal congenital...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690743/ https://www.ncbi.nlm.nih.gov/pubmed/23840219 http://dx.doi.org/10.1155/2013/404710 |
_version_ | 1782274397997891584 |
---|---|
author | Şeker Koçkara, Ayşe Kayataş, Mansur Huzmeli, Can Candan, Ferhan Gümüş, Cesur |
author_facet | Şeker Koçkara, Ayşe Kayataş, Mansur Huzmeli, Can Candan, Ferhan Gümüş, Cesur |
author_sort | Şeker Koçkara, Ayşe |
collection | PubMed |
description | Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is responsible for 8–10% of patients with end-stage renal failure. The major extrarenal complications of ADPKD are cardiovascular abnormalities. Interrupted aortic arch (IAA) is a lethal congenital cardiac abnormality seen with a frequency of 3/1000000 births and is defined as a segment of the arcus aorta being atresic. In the literature, there are no any reports showing that polycystic kidney disease and interrupted aortic arch occur together. In this study, we present a rare case in which the patient has polycystic kidney disease and IAA together and discuss whether IAA is a complication of ADPKD. |
format | Online Article Text |
id | pubmed-3690743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36907432013-07-09 Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease Şeker Koçkara, Ayşe Kayataş, Mansur Huzmeli, Can Candan, Ferhan Gümüş, Cesur Case Rep Med Case Report Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is responsible for 8–10% of patients with end-stage renal failure. The major extrarenal complications of ADPKD are cardiovascular abnormalities. Interrupted aortic arch (IAA) is a lethal congenital cardiac abnormality seen with a frequency of 3/1000000 births and is defined as a segment of the arcus aorta being atresic. In the literature, there are no any reports showing that polycystic kidney disease and interrupted aortic arch occur together. In this study, we present a rare case in which the patient has polycystic kidney disease and IAA together and discuss whether IAA is a complication of ADPKD. Hindawi Publishing Corporation 2013 2013-06-09 /pmc/articles/PMC3690743/ /pubmed/23840219 http://dx.doi.org/10.1155/2013/404710 Text en Copyright © 2013 Ayşe Şeker Koçkara et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Şeker Koçkara, Ayşe Kayataş, Mansur Huzmeli, Can Candan, Ferhan Gümüş, Cesur Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title | Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title_full | Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title_fullStr | Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title_full_unstemmed | Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title_short | Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease |
title_sort | interrupted aortic arch in an adult with polycystic kidney disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690743/ https://www.ncbi.nlm.nih.gov/pubmed/23840219 http://dx.doi.org/10.1155/2013/404710 |
work_keys_str_mv | AT sekerkockaraayse interruptedaorticarchinanadultwithpolycystickidneydisease AT kayatasmansur interruptedaorticarchinanadultwithpolycystickidneydisease AT huzmelican interruptedaorticarchinanadultwithpolycystickidneydisease AT candanferhan interruptedaorticarchinanadultwithpolycystickidneydisease AT gumuscesur interruptedaorticarchinanadultwithpolycystickidneydisease |