2016Cardiology ResearchOpen access

Cardiac Amyloidosis Masked as Hypertrophic Cardiomyopathy: A Case Report

Jing Wang, Amy Marzolf, Janet C.L. Zhang, Anjali Owens, Yuchi Han

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Abstract

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

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Available abstract

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

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