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Isolated interrupted aortic arch, a rare cause of hypertension in adults

Date
2008
Author
Dogan, S. M.
Aydin, Mustafa
Hekimoglu, Koray
Gungorduk, Alper
Yildirim, Nesligul
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Abstract
Interrupted aortic arch (IAA) is a rare and usually lethal congenital malformation. Patients with complete IAA very rarely do reach adult age without previous surgical intervention. The present report describes a 26-year-old asymptomatic isolated IAA case with hypertension that was incidentally diagnosed. IAA just distal to the left subclavian artery and a markedly developed collateral circulation was demonstrated by cardiac catheterization and thoracic 3D magnetic resonance angiography. This case report was also interesting that only mild arterial hypertension of the upper extremities was incidentally found in the patient. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
URI
http://hdl.handle.net/20.500.12627/26799
https://doi.org/10.1016/j.ijcard.2007.04.008
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Creative Commons Lisansı

İstanbul Üniversitesi Akademik Arşiv Sistemi (ilgili içerikte aksi belirtilmediği sürece) Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV