Ascending aortic coarctation-an atypical location in a non-takayasu arteritis female patient

dc.authorid0000-0001-5889-2257
dc.authorid0000-0001-7575-5297
dc.authorid0000-0001-6602-5946
dc.authorid0000-0001-9191-952X
dc.authorid0000-0002-0600-5801
dc.authorid0000-0003-4856-0974
dc.contributor.authorÖteyaka, Emre
dc.contributor.authorKuğuoğlu, Okan Eren
dc.contributor.authorSarı, Gizem
dc.contributor.authorBasunlu, Mehmet Turan
dc.contributor.authorDoğan, Mehmet Sait
dc.contributor.authorÇalış, Elif
dc.contributor.authorHakgör, Aykun
dc.contributor.authorTürkoğlu, Halil
dc.contributor.authorUğurlucan, Murat
dc.date.accessioned2023-09-08T08:42:44Z
dc.date.available2023-09-08T08:42:44Z
dc.date.issued2023
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kalp ve Damar Cerrahisi Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Kardiyoloji Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Radyoloji Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Tıbbi Patoloji Ana Bilim Dalı
dc.description.abstractCoarctation of the aorta is a well-known congenital cardiovascular disorder that typically occurs within proximity to the ductus arteriosus. The ascending aorta, distal descending aorta, and abdominal aorta are segments which are prone to development of an atypical coarctation. The etiologies of atypical cases are usually associated with various types of vasculitis syndromes or underlying genetic disorders. In this report, we present a 24-year-old female patient with an ascending aortic coarctation which developed secondary to an atherosclerotic process.
dc.identifier.citationÖteyaka, E., Kuğuoğlu, O. E., Sarı, G., Basunlu, M. T., Doğan, M. S., Çalış, E. ... Uğurlucan, M. (2023). Ascending aortic coarctation-an atypical location in a non-takayasu arteritis female patient. Brazilian Journal of Cardiovascular Surgery, 38(4). https://dx.doi.org/10.21470/1678-9741-2022-0268
dc.identifier.doi10.21470/1678-9741-2022-0268
dc.identifier.issn0102-7638
dc.identifier.issn1678-9741
dc.identifier.issue4
dc.identifier.pmid37402277
dc.identifier.scopus2-s2.0-85164243552
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://dx.doi.org/10.21470/1678-9741-2022-0268
dc.identifier.urihttps://hdl.handle.net/20.500.12511/11396
dc.identifier.volume38
dc.identifier.wos001043093600005en_US
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorÖteyaka, Emre
dc.institutionauthorKuğuoğlu, Okan Eren
dc.institutionauthorSarı, Gizem
dc.institutionauthorBasunlu, Mehmet Turan
dc.institutionauthorDoğan, Mehmet Sait
dc.institutionauthorÇalış, Elif
dc.institutionauthorHakgör, Aykun
dc.institutionauthorTürkoğlu, Halil
dc.language.isoen
dc.publisherSociedade Brasileira de Cirurgia Cardiovascular
dc.relation.ispartofBrazilian Journal of Cardiovascular Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsAttribution 4.0 International*
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectAortic Coarctation
dc.subjectAtherosclerosis
dc.subjectTakayasu Arteritis
dc.titleAscending aortic coarctation-an atypical location in a non-takayasu arteritis female patient
dc.typeArticle

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