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A rare cause of dyspnea: Isolated congenitally corrected transposition of the great arteries

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dc.contributor.author Ulutas, Zeynep
dc.contributor.author Yildirim, Erkan
dc.contributor.author Abdelrahman, Hasan
dc.contributor.author Hidayet, Siho
dc.date.accessioned 2022-03-15T15:46:20Z
dc.date.available 2022-03-15T15:46:20Z
dc.date.issued 2021
dc.identifier.citation Ulutas, Z., Yildirim, E., Abdelrahman, H., & Hidayet, S. (2021). A rare cause of dyspnea: Isolated congenitally corrected transposition of the great arteries. Annals of Medical Research en_US
dc.identifier.uri http://hdl.handle.net/11616/55749
dc.description.abstract Corrected transposition of the great arteries is a rare pathology with an incidence of 1% among the congenital heart diseases. It is thought to have multifactorial inheritance. It is mostly seen in men. If there is no concomitant pathology, the blood flow is physiological and does not show symptoms until advanced ages. Life expectancy is close to normal in those with isolated pathology. Risk factors determining mortality include progressive right ventricular dysfunction, AV block, and severe tricuspid insufficiency. In this case, we present a CCTGA patient with dyspnea symptoms without any additional pathology. en_US
dc.language.iso eng en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title A rare cause of dyspnea: Isolated congenitally corrected transposition of the great arteries en_US
dc.type article en_US
dc.relation.journal Annals of Medical Research en_US
dc.contributor.department İnönü Üniversitesi en_US


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