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...
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| Format: | Article |
| Language: | English |
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Wiley
2013-01-01
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| Series: | Case Reports in Medicine |
| Online Access: | http://dx.doi.org/10.1155/2013/404710 |
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| author | Ayşe Şeker Koçkara Mansur Kayataş Can Huzmeli Ferhan Candan Cesur Gümüş |
| author_facet | Ayşe Şeker Koçkara Mansur Kayataş Can Huzmeli Ferhan Candan Cesur Gümüş |
| author_sort | Ayşe Şeker Koçkara |
| collection | DOAJ |
| 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 | Article |
| id | doaj-art-148e6361c0464f0a81c1f6d8384f16ec |
| institution | Kabale University |
| issn | 1687-9627 1687-9635 |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Case Reports in Medicine |
| spelling | doaj-art-148e6361c0464f0a81c1f6d8384f16ec2025-02-03T05:44:49ZengWileyCase Reports in Medicine1687-96271687-96352013-01-01201310.1155/2013/404710404710Interrupted Aortic Arch in an Adult with Polycystic Kidney DiseaseAyşe Şeker Koçkara0Mansur Kayataş1Can Huzmeli2Ferhan Candan3Cesur Gümüş4Department of Nephrology, Cumhuriyet University Medical School, 58140 Sivas, TurkeyDepartment of Nephrology, Cumhuriyet University Medical School, 58140 Sivas, TurkeyDepartment of Nephrology, Cumhuriyet University Medical School, 58140 Sivas, TurkeyDepartment of Nephrology, Cumhuriyet University Medical School, 58140 Sivas, TurkeyDepartment of Radiology, Cumhuriyet University Medical School, 58140 Sivas, TurkeyAutosomal 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.http://dx.doi.org/10.1155/2013/404710 |
| spellingShingle | Ayşe Şeker Koçkara Mansur Kayataş Can Huzmeli Ferhan Candan Cesur Gümüş Interrupted Aortic Arch in an Adult with Polycystic Kidney Disease Case Reports in Medicine |
| 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 |
| url | http://dx.doi.org/10.1155/2013/404710 |
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