Diagnostic algorithm in transthyretin amyloidosis with cardiomyopathy

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
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
Series:Българска кардиология
Subjects:
transthyretin amyloidosis
cardiomyopathy
diagnos
Online Access:https://journal.bgcardio.org/article/53407/download/pdf/

Internet

https://journal.bgcardio.org/article/53407/download/pdf/

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