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Right ventricular hypoplasia and aortic stenosis: Autopsy case

dc.contributor.authorBülent, E.
dc.contributor.authorTurkmen, N.
dc.contributor.authorFedakar, R.
dc.contributor.buuauthorTÜRKMEN İNANIR, NURSEL
dc.contributor.buuauthorFEDAKAR, RECEP
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentAdli Tıp Ana Bilim Dalı
dc.contributor.scopusid25644912700
dc.contributor.scopusid8715251700
dc.contributor.scopusid8725968900
dc.date.accessioned2025-08-06T23:44:21Z
dc.date.issued2008-11-01
dc.description.abstractNeonatal cardiac malformation cases mostly need surgical repair. It is important to describe the morphological features of these malformations. A 3 months-old baby girl was brought to a local clinic after three days antibiotic therapy. No signs of life were present. Autopsy findings showed adhesion of right ventricular surfaces which caused the chamber volume to significantly decrease. The ventricular wall was thinned, out and become crescent shaped. This rare autopsy case, with right ventricle hypoplasia and severe stenosis of aorta is presented.
dc.identifier.endpage 647
dc.identifier.issn0030-9982
dc.identifier.issue11
dc.identifier.scopus2-s2.0-56049098790
dc.identifier.startpage645
dc.identifier.urihttps://hdl.handle.net/11452/54067
dc.identifier.volume58
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalJournal of the Pakistan Medical Association
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleRight ventricular hypoplasia and aortic stenosis: Autopsy case
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/ Adli Tıp Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublicationb47dba7f-e6a6-4844-a4de-3d51ee5a82c4
relation.isAuthorOfPublication64310c17-8b59-40c0-8b34-8de15da2a3da
relation.isAuthorOfPublication.latestForDiscoveryb47dba7f-e6a6-4844-a4de-3d51ee5a82c4

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