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dc.contributor.authorDogan, S. M.
dc.contributor.authorAydin, Mustafa
dc.contributor.authorHekimoglu, Koray
dc.contributor.authorGungorduk, Alper
dc.contributor.authorYildirim, Nesligul
dc.date.accessioned2021-03-03T10:02:13Z
dc.date.available2021-03-03T10:02:13Z
dc.date.issued2008
dc.identifier.citationYildirim N., Dogan S. M. , Aydin M., Hekimoglu K., Gungorduk A., "Isolated interrupted aortic arch, a rare cause of hypertension in adults", INTERNATIONAL JOURNAL OF CARDIOLOGY, cilt.127, sa.2, 2008
dc.identifier.issn0167-5273
dc.identifier.otherav_2050bf88-dffe-48d0-abeb-aff8b045ca7f
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/26799
dc.identifier.urihttps://doi.org/10.1016/j.ijcard.2007.04.008
dc.description.abstractInterrupted 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.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKardiyoloji
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleIsolated interrupted aortic arch, a rare cause of hypertension in adults
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF CARDIOLOGY
dc.contributor.departmentZonguldak Bülent Ecevit Üniversitesi , ,
dc.identifier.volume127
dc.identifier.issue2
dc.contributor.firstauthorID89377


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