Purpose Coding mutations in the Transthyretin (TTR) gene cause a hereditary form of
amyloidosis characterized by a complex genotype-phenotype correlation with limited …

Restrictive cardiomyopathy secondary to cardiac amyloidosis is an underdiagnosed cause
of heart failure and it is associated with significant morbidity and mortality. The most common …

Amyloidosis is the result of the extracellular deposition of amyloid in various organs.
Common types are light-chain and transthyretin amyloidosis. Cardiac amyloidosis (CA) is a …

Cardiac amyloidosis is caused by the extracellular, interstitial deposition of misfolded protein
deposits or amyloid fibrils that result in a restrictive cardiomyopathy with associated …

Cardiac amyloidosis (CA) is an underdiagnosed disease with rapid progression and short
overall survival. Despite therapeutic advances, resource-limited settings including India are …