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How Tafamidis and RNA Therapies Are Changing the ATTR-CM Landscape
Transthyretin Amyloid Cardiomyopathy (ATTR-CM) is a progressive, often underdiagnosed form of restrictive cardiomyopathy caused by the deposition of misfolded transthyretin (TTR) protein in the myocardium. Affecting both genetic and aging populations, ATTR-CM has emerged as a critical and increasingly recognized cause of heart failure with preserved ejection fraction (HFpEF), particularly in...
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