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Öğe An isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case report(Wiley, 2022) Demir, Muhammed; Akdag, Serkan; Deniz, Mehmet Akif; Simsek, HakkiUnilateral 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.
