Diagnostic algorithm in transthyretin amyloidosis with cardiomyopathy

Transthyretin cardiac amyloidosis is a restrictive cardiomyopathy ((ATTR-CM), caused by an extracellular deposition of insoluble amyloid fibrils in the myocardium. It is a life threatening disease with life expectancy of 2 to 6 years after diagnosis. There are two types – hereditary and wild type. R...

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Bibliographic Details

Published in:	Българска кардиология
Main Authors:	Mariana Gospodinova, Elena Kinova, Iana Simova, Yoto Yotov, Marina Garcheva, Galina Kirova, Kamelia Genova, Albena Todorova, Stayko Sarafov, Ivailo Tournev, Mariya Tokmakova, Vasil Velchev
Format:	Article
Language:	Bulgarian
Published:	Pensoft Publishers 2020-07-01
Subjects:	transthyretin amyloidosis cardiomyopathy diagnos
Online Access:	https://journal.bgcardio.org/article/53407/download/pdf/