APICAL VARIANT HYPERTROPHIC CARDIOMYOPATHY PRESENTS AS MID-CAVITARY HYPERTROPHIC CARDIOMYOPATHY WITH OBSTRUCTION 10 YEARS LATER

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