Transthyretin-Related Amyloid Cardiomyopathy (ATTR-CM)
Transthyretin-related amyloid cardiomyopathy (ATTR-CM) is a progressive, life-threatening form of cardiac amyloidosis caused by the deposition of misfolded transthyretin (TTR) protein in the myocardium. This condition leads to restrictive cardiomyopathy, diastolic heart failure, and ultimately, significant morbidity and mortality if left untreated. ATTR-CM can occur in two main forms: Pathogenesis and Molecular Mechanism TTR is