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Noninvasive diagnosis of hereditary transthyretin-related cardiac amyloidosis: A case report

RATIONALE: Cardiac transthyretin amyloidosis is a progressive and fatal cardiomyopathy for which several promising therapies are in development. The diagnosis is frequently delayed or missed because of the limited specificity of clinical manifestations, routine electrocardiogram, echocardiography an...

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Bibliografiske detaljer
Udgivet i:Medicine (Baltimore)
Main Authors: Qin, Jin, Zhan, Chenao, Li, Haojie, Han, Yunfeng, Wang, Hong, Li, Rui, Ma, Fei, Yan, Jiangtao
Format: Artigo
Sprog:Inglês
Udgivet: Wolters Kluwer Health 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6709038/
https://ncbi.nlm.nih.gov/pubmed/31348283
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016566
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