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Intramyocardial calcification in apical hypertrophic cardiomyopathy assessed using multimodality imaging: a case series
Introduction Apical hypertrophic cardiomiopathy (ApHCM) is an HCM variant, first described by Sakamoto et al. in 1976, accounting for up to 25% of HCM in Asian population and 1–10% in non-Asian one and affects frequently males in midlife.1 It is more sporadic and less sarcomere mutation associated,1 than classic HCM.
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