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dc.contributor.authorAydin, Unal
dc.contributor.authorBAKIR, İhsan
dc.contributor.authorKahraman, Zeynep
dc.contributor.authorOnan, Burak
dc.date.accessioned2022-02-18T09:14:26Z
dc.date.available2022-02-18T09:14:26Z
dc.date.issued2017
dc.identifier.citationOnan B., Aydin U., Kahraman Z., BAKIR İ., "Robotic surgery for atrial septal defect closure in a case of Kabuki syndrome", TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY, cilt.45, sa.1, ss.77-81, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_28607731-59de-4006-a0d9-90965718ee36
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176815
dc.identifier.urihttps://doi.org/10.5543/tkda.2016.84554
dc.description.abstractKabuki syndrome is a rare congenital malformation syndrome characterized by mental retardation, skeletal deformities, auditory dysfunction, cardiac defects, and distinctive facial appearance. Although complex cardiovascular malformations present in early childhood, rarely, atrioventricular septal defects may also present in young adults. Presently described is case of a 22-year-old female with KS who presented with ostium secundum atrial septal defect with deficient rim and idiopathic thrombocytopenic purpura. In this case, minimally invasive robotic surgery was preferred for closure of atrial septal defect.
dc.language.isoeng
dc.subjectCardiology and Cardiovascular Medicine
dc.subjectHealth Sciences
dc.subjectSağlık Bilimleri
dc.subjectKardiyoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleRobotic surgery for atrial septal defect closure in a case of Kabuki syndrome
dc.typeMakale
dc.relation.journalTURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY
dc.contributor.departmentIstanbul Mehmet Akif Ersoy Thorac & Cardiovasc Ho , ,
dc.identifier.volume45
dc.identifier.issue1
dc.identifier.startpage77
dc.identifier.endpage81
dc.contributor.firstauthorID3385207


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