Publication:
A very rare case of coexistence of ventricular noncompaction cardiomyopathy, myocardial bridging and atherosclerosis.

dc.contributor.authorErdogan, Ercan
dc.contributor.authorAkkaya, Mehmet
dc.contributor.authorBacaksiz, Ahmet
dc.contributor.authorTasal, Abdurrahman
dc.contributor.authorSevgili, Emrah
dc.date.accessioned2023-05-16T16:46:21Z
dc.date.available2023-05-16T16:46:21Z
dc.description.abstractNoncompaction of the ventricular myocardium is a rare congenital heart disease, presumably caused by the intrauterine arrest of the myocardial compaction process at the beginning of fetal development. It could remain asymptomatic or manifest with congestive heart failure, arrhythmias, and systemic thromboemboli. Here we report a 55-year-old man who was admitted to hospital with chest pain and dyspnea, whose further evaluation revealed left ventricular noncompaction cardiomyopathy accompanying myocardial bridging and stenosis of the right coronary artery.
dc.identifier.doi10.5114/pwki.2013.35455
dc.identifier.pubmed24570713
dc.identifier.scopus84880120414
dc.identifier.urihttps://hdl.handle.net/20.500.12645/38214
dc.identifier.wosWOS:000321600600012
dc.language.isoen
dc.subjectatherosclerosis
dc.subjectmyocardial bridging
dc.subjectventricular noncompaction
dc.titleA very rare case of coexistence of ventricular noncompaction cardiomyopathy, myocardial bridging and atherosclerosis.
dspace.entity.typePublication
local.indexed.atPubMed

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