Cardiac amyloidosis (CA) is a progressive infiltrative disease caused most commonly by the deposition of misfolded, cleaved and aggregated monoclonal immunoglobulin free light chain (AL) or transthyretin (ATTR) proteins in the myocardial extracellular space [1]. Recent advances in imaging techniques and the development of an algorithm for non-invasive confirmation of ATTR-CA [2] have transformed the diagnosis of this condition.
Editorial for the article: Hospitalization-based epidemiology of systemic and cardiac amyloidosis in the Veneto Region, Italy
Porcari, Aldostefano
;Pozzan, Marco
2024-01-01
Abstract
Cardiac amyloidosis (CA) is a progressive infiltrative disease caused most commonly by the deposition of misfolded, cleaved and aggregated monoclonal immunoglobulin free light chain (AL) or transthyretin (ATTR) proteins in the myocardial extracellular space [1]. Recent advances in imaging techniques and the development of an algorithm for non-invasive confirmation of ATTR-CA [2] have transformed the diagnosis of this condition.File in questo prodotto:
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