Apical variant hypertrophic cardiomyopathy (AHCM) is a rare genetic disease with variable phenotypic expression, typically associated with a benign prognosis. A 71-year-old female with AHCM presented with 3 days of… Click to show full abstract
Apical variant hypertrophic cardiomyopathy (AHCM) is a rare genetic disease with variable phenotypic expression, typically associated with a benign prognosis. A 71-year-old female with AHCM presented with 3 days of exertional chest pain and was found to have NSTEMI. EKG showed deep T-wave
               
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