Cardiac compromise due to AL amyloidosis: dissimilarity as an attribute. Report of 3 cases

AL amyloidosis (formerly called primary amyloidosis) is a rare systemic entity, with an unknown incidence in the world, which can develop heart involvement in almost half of patients, leading to restrictive cardiomyopathy by amyloid tissue deposit. We present 3 cases of patients who consulted for ac...

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Bibliographic Details
Main Authors: Julián Rondón-Carvajal, Kelly Johanna Betancur-Salazar
Format: Article
Language:Spanish
Published: Universidad de Antioquia 2021-01-01
Series:Iatreia
Subjects:
Online Access:https://revistas.udea.edu.co/index.php/iatreia/article/view/340918/20802493