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Cardiac Amyloidosis Masked as Hypertrophic Cardiomyopathy: A Case Report

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.

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Pubblicato in:Cardiol Res
Autori principali: Wang, Jing, Marzolf, Amy, Zhang, Janet C. L., Owens, Anjali, Han, Yuchi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elmer Press 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5295565/
https://ncbi.nlm.nih.gov/pubmed/28197289
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14740/cr496w
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