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Reverse cardiac remodelling and dysfunction in A97S transthyretin cardiac amyloidosis after tafamidis treatment

Abstract Transthyretin cardiomyopathy (ATTR‐CM) is an under‐recognized cause of heart failure, but it has received increasing attention due to the availability of treatment options. We present a case of hereditary transthyretin cardiomyopathy (A97S, an under‐represented variant in current clinical s...

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Furkejuvvon:
Váldodahkkit: Yuan‐Kun (Aden) Wu, Cheng‐Hsuan Tsai, Mao‐Yuan Su, Chi‐Chao Chao, Mei‐Fang Cheng, Chia‐Tung Shun, Sung‐Tsang Hsieh, Yen‐Hung Lin
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: Oxford University Press 2022-12-01
Ráidu:ESC Heart Failure
Fáttát:
Cardiac amyloidosis
Tafamidis
Echocardiography
Cardiac magnetic resonance imaging
Technetium‐99m pyrophosphate scintigraphy
Liŋkkat:https://doi.org/10.1002/ehf2.14165
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