Homozygous Familial Hypercholesterolaemia with Valvular Aortic Stenosis and Significant Coronary Artery Disease: A Case Report.

dc.contributor.authorDutta
dc.contributor.authorIslam, A K M M
dc.contributor.authorUllah, M
dc.contributor.authorZaman, A
dc.contributor.authorKarmakar, K K
dc.contributor.authorKundu, S K
dc.date.accessioned2015-12-16T09:14:32Z
dc.date.available2015-12-16T09:14:32Z
dc.date.issued2014
dc.description.abstractHomozygous Familial Hypercholesterolaemia is a genetic disorder which usually presents with early cardiovascular disease ranging from premature ischaemic disease, including myocardial infarction to aortic root stenosis. A 21 year old Bangladeshi male presented with exertional chest pain and breathlessness. He was diagnosed as a case of Homozygous Familial Hypercholesterolaemia. His angina symptoms were due to underlying valvular aortic stenosis which is a rare presentation of Homozygous Familial Hypercholesterolaemia.en_US
dc.identifier.citationDutta, Islam A K M M, Ullah M, Zaman A, Karmakar K K, Rahman M Z, Kundu S K. Homozygous Familial Hypercholesterolaemia with Valvular Aortic Stenosis and Significant Coronary Artery Disease: A Case Report. Cardiovascular Journal. 2014; 6(2): 180-183.en_US
dc.identifier.issn2071-0917
dc.identifier.issn2309-6357
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/168307
dc.language.isoenen_US
dc.source.urihttps://banglajol.info/index.php/CARDIO/article/view/18365en_US
dc.subjectHomozygous Familial Hypercholesterolaemiaen_US
dc.subjectGenetic disorderen_US
dc.subjectMyocardial infarctionen_US
dc.subjectValvular aortic stenosisen_US
dc.titleHomozygous Familial Hypercholesterolaemia with Valvular Aortic Stenosis and Significant Coronary Artery Disease: A Case Report.en_US
dc.typeArticleen_US
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