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.

27 August 2021 (00:00 - 00:00)
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Congress Presentation Part of: Acute and chronic heart failure Chronic Heart Failure ESC Premium Access ESC Congress 2021 - The Digital Experience

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