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Absence of Right Superior Vena Cava and Aortic Annular Hypoplasia in a Patient With Turner's Syndrome

dc.authorid Kutay, Veysel/0000-0002-5822-5259
dc.authorscopusid 6602259733
dc.authorscopusid 7005925621
dc.contributor.author Kutay, V
dc.contributor.author Yakut, C
dc.date.accessioned 2025-05-10T17:45:05Z
dc.date.available 2025-05-10T17:45:05Z
dc.date.issued 2005
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Yuzuncu Yil Univ, Fac Med, Cardiovasc Surg Clin, Van, Turkey en_US
dc.description Kutay, Veysel/0000-0002-5822-5259 en_US
dc.description.abstract Cardiovascular abnormalities are frequently encountered in patients with Turner's syndrome. These include coarctation of the aorta, bicuspid aortic valve, aortic root dilatation, atrial and ventricular septal defects, but absence of the right superior vena cava (SVC) in visceroatrial situs solitus is extremely rare. We report absence of the right SVC and congenital aortic annular hypoplasia with bicuspid aortic valve stenosis in a patient with Turner's syndrome. Aortic root extension with prosthetic valve replacement was performed and absent right SVC, which was detected incidentally during operation, is confirmed by postoperative venous angiogram. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1111/j.1540-8191.2005.200462.x
dc.identifier.endpage 376 en_US
dc.identifier.issn 0886-0440
dc.identifier.issn 1540-8191
dc.identifier.issue 4 en_US
dc.identifier.pmid 15985143
dc.identifier.scopus 2-s2.0-22244486984
dc.identifier.scopusquality Q3
dc.identifier.startpage 375 en_US
dc.identifier.uri https://doi.org/10.1111/j.1540-8191.2005.200462.x
dc.identifier.uri https://hdl.handle.net/20.500.14720/16238
dc.identifier.volume 20 en_US
dc.identifier.wos WOS:000231343000018
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.relation.publicationcategory Diğer en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Absence of Right Superior Vena Cava and Aortic Annular Hypoplasia in a Patient With Turner's Syndrome en_US
dc.type Editorial en_US

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