Demir, MuhammedAkdag, SerkanDeniz, Mehmet AkifSimsek, Hakki2024-04-242024-04-2420220742-28221540-8175https://doi.org/10.1111/echo.15450https://hdl.handle.net/11468/17528Unilateral absence of pulmonary artery (UAPA) resulting from a defect in the aortic arch's embryogenesis. Patients who survive into adulthood is rare. Herein, we presented a case of UAPA with pulmonary hypertension in a 49-year old female.eninfo:eu-repo/semantics/closedAccessCongenital Heart DiseaseCoronary Artery Collaterals IntroductionPulmonary Artery AgenesisAn isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case reportAn isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case reportEditorial391013671369WOS:0008532998000012-s2.0-851378538153610081410.1111/echo.15450Q3Q4