Cardiac Amyloidosis Masked as Hypertrophic Cardiomyopathy: A Case Report
Jing Wang, Amy Marzolf, Janet C.L. Zhang, Anjali Owens, Yuchi Han
Abstract
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Jing Wang, Amy Marzolf, Janet C.L. Zhang, Anjali Owens, Yuchi Han
Abstract
Open-access reader
It is well known that cardiac amyloidosis and hypertrophic cardiomyopathy (HCM) have different physiologies and pathologies. However, it might be difficult to differentiate cardiac amyloidosis from HCM in certain clinical situations. Cardiol Res. 2016;7(5):178-180 doi: http://dx.doi.org/10.14740/cr496w
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It is well known that cardiac amyloidosis and hypertrophic cardiomyopathy (HCM) have different physiologies and pathologies. However, it might be difficult to differentiate cardiac amyloidosis from HCM in certain clinical situations. Cardiol Res. 2016;7(5):178-180 doi: http://dx.doi.org/10.14740/cr496w
Key concepts: Medicine, Hypertrophic cardiomyopathy, Cardiology, Internal medicine, Cardiac amyloidosis, Amyloidosis, Cardiomyopathy, Restrictive cardiomyopathy