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Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

<b>Background/Objectives</b>: Cardiac amyloidosis (CA) is an underdiagnosed and potentially life-threatening infiltrative cardiomyopathy characterized by the extracellular deposition of misfolded amyloid fibrils in cardiac tissue. It is most commonly associated with light-chain (AL) amyloidosis and...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Dana Emilia Movila, Alexandru Catalin Motofelea, Dragos Cozma, Oana Albai, Alexandra Christa Sima, Minodora Andor, Tudor Ciocarlie, Simona Ruxanda Dragan
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI AG 2025-05-01
Schriftenreihe:Biomedicines
Schlagworte:
amyloidosis
cardiac amyloidosis
diagnosis
TTR
transthyretin
Online-Zugang:https://www.mdpi.com/2227-9059/13/5/1230
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