Cardiac transthyretin amyloidosis in patients with conduction system disease
Presentation
Cardiac transthyretin amyloidosis in patients with conduction system disease
Presentation
Familial dilated cardiomyopathy caused by the mutation of the ANKRD1 gene - a case report of severe left ventricular systolic dysfunction with EF of 20% treated with sacubitril/valsartan and complete reverse remodeling.
