An isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case report

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dc.contributor.authorDemir, Muhammed
dc.contributor.authorAkdag, Serkan
dc.contributor.authorDeniz, Mehmet Akif
dc.contributor.authorSimsek, Hakki
dc.date.accessioned2024-04-24T17:11:27Z
dc.date.available2024-04-24T17:11:27Z
dc.date.issued2022
dc.departmentDicle Üniversitesien_US
dc.description.abstractUnilateral 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.en_US
dc.identifier.doi10.1111/echo.15450
dc.identifier.endpage1369en_US
dc.identifier.issn0742-2822
dc.identifier.issn1540-8175
dc.identifier.issue10en_US
dc.identifier.pmid36100814
dc.identifier.scopus2-s2.0-85137853815
dc.identifier.scopusqualityQ3
dc.identifier.startpage1367en_US
dc.identifier.urihttps://doi.org/10.1111/echo.15450
dc.identifier.urihttps://hdl.handle.net/11468/17528
dc.identifier.volume39en_US
dc.identifier.wosWOS:000853299800001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofEchocardiography-A Journal of Cardiovascular Ultrasound and Allied Techniques
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital Heart Diseaseen_US
dc.subjectCoronary Artery Collaterals Introductionen_US
dc.subjectPulmonary Artery Agenesisen_US
dc.titleAn isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case reporten_US
dc.titleAn isolated congenital absence of right pulmonary artery associated with pulmonary hypertension with coronary collaterals: A case report
dc.typeEditorialen_US

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