Restrictive cardiomyopathy due to cardiac amyloidosis: case report

https://doi.org/10.36109/rmg.v161i4.571
Restrictive cardiomyopathy thromboembolism. Amyloidosis

Authors

  • José Gómez
    jalgox120490@gmail.com
    Unidad de Cardiología, Hospital Roosevelt, Guatemala, Guatemala., Guatemala
  • Romeo Tereta Unidad de Cardiología, Hospital Roosevelt, Guatemala, Guatemala., Guatemala
  • Lubeck Herrera Unidad de Cardiología, Hospital Roosevelt, Guatemala, Guatemala., Guatemala
  • Rodolfo Gutiérrez Unidad de Cardiología, Hospital Roosevelt, Guatemala, Guatemala., Guatemala
Vol. 161 No. 4: October - December, 2022
Case Report
July 31, 2022
December 11, 2022

Cardiac amyloidosis is a disorder caused by the deposition of amyloid fibrils in the extracellular space of the myocardium, presenting with heart failure with preserved systolic function and progressing to typical restrictive physiology, syncope, atria

How to Cite

Restrictive cardiomyopathy due to cardiac amyloidosis: case report. (2022). Revista médica (Colegio De Médicos Y Cirujanos De Guatemala), 161(4), 416-418. https://doi.org/10.36109/rmg.v161i4.571