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A rare coexistence: Type 1 congenital intrahepatic portosystemic shunt in a patient with non-compaction cardiomyopathy

By Serkan Duyuler, Pınar Türker Duyuler and Ali Çoner

Abstract

AbstractNon-compaction cardiomyopathy is described by the spongy appearance of myocardium and this condition frequently exists with other cardiac or extracardiac abnormalities. However, coexistence of non-compaction cardiomyopathy with congenital intrahepatic porto-systemic shunt was not reported previously. Here we presented a 22-year-old male patient with Type 1 congenital intrahepatic porto-systemic shunt and non-compaction cardiomyopathy

Year: 2016
DOI identifier: 10.1016/j.ijcac.2016.08.005
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