Author/Authors :
Peighambari, Mehdi tehran university of medical sciences tums - Rajaie Cardiovascular Medical and Research Center, تهران, ايران , Parsaei, Mozghan tehran university of medical sciences tums - Rajaie Cardiovascular Medical and Research Center, تهران, ايران , Sadeghpour, Anita tehran university of medical sciences tums - Rajaie Cardiovascular Medical and Research Center, تهران, ايران , Alizadehasl, Azin tabriz university of medical sciences - Cardiovascular Research Center, ايران
Abstract :
Apical Hypertrophic Cardiomyopathy is an uncommon condition constituting 1% -2% of the cases with Hypertrophic Cardiomyopathy (HCM) diagnosis. We interestingly report two patients with apical hypertrophic cardiomyopathy in association with significant pulmonary artery hypertension without any other underlying reason for pulmonary hypertension. The patients were assessed by echocardiography, cardiac catheterization and pulmonary function parameters study.