OPEN ACCESS
Abstract (provisional)
Hypertrophic cardiomyopathy (HCM) is one of the most common inherited cardiomyopathy. The identification of patients with HCM is sometimes still a challenge. Moreover, the pathophysiology of HCM is complex because of left ventricular hyper-contractile state, diastolic dysfunction, ischemia and obstruction which often are coexistent in the same patient. In this review, we discuss the current and emerging echocardiographic methodology that can help physicians in the correct diagnostic and pathophysiological assessment of patients with HCM.FULL TEXT PDF
No comments:
Post a Comment