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dc.contributor.authorEmet, Samim
dc.contributor.authorYalin, Kivanc
dc.contributor.authorUcar, Serra
dc.contributor.authorAkpinar, Timur Selcuk
dc.contributor.authorKose, Murat
dc.date.accessioned2021-03-05T08:38:34Z
dc.date.available2021-03-05T08:38:34Z
dc.identifier.citationKose M., Ucar S., Emet S., Akpinar T. S. , Yalin K., "A Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy", CASE REPORTS IN CARDIOLOGY, 2015
dc.identifier.otherav_99eb68c5-09b1-4be6-a18f-720d7ad336e7
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/103505
dc.identifier.urihttps://doi.org/10.1155/2015/935253
dc.description.abstractThe aortopulmonary window (APW) is an abnormal communication between the ascending aorta and the pulmonary trunk in the presence of two separate semilunar valves. It is a rare congenital malformation which represents 0.1% of all congenital cardiac diseases. Herein, we report a very rare case of 27-year-old patient with unrepaired APW causing Eisenmenger syndrome and pulmonary hypertension who was asymptomatic until her first pregnancy. The median survival of uncorrected APW is 33 years. Aortopulmonary window is a very rare congenital anomaly. To our knowledge, asymptomatic adult case has not been reported until now. APW should be considered in the differential diagnosis of the severe pulmonary hypertension also in adult patients.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKardiyoloji
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectKlinik Tıp
dc.titleA Case of Aortopulmonary Window: Asymptomatic until the First Pregnancy
dc.typeMakale
dc.relation.journalCASE REPORTS IN CARDIOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.contributor.firstauthorID84798


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