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Cardiac Amyloidosis (Transthyretin-Associated Familial Amyloidosis)

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Clinical Guide to Cardiovascular Disease
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Abstract

Consider this Diagnosis in any patient with Heart Failure and preserved ejection fraction

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Review: TTR

AL LV Function

Amyloidogenic V122I Transthyretin Variant in African Americans

Conduction Abnormalities/Atrial Arrhythmias

High-Sensitivity Troponin T

Intracardiac Thrombus/Anticoagulation

LGE

LVOT Obstruction: Differentiation from HCM

MRI Differentiation: AL vs TTR

Tafamadis Meglumine

TTR Transthyretin-Associated Familial Amyloidosis: Exclusive Card Phenotype

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© 2016 Springer-Verlag London

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Friedewald, V.E. (2016). Cardiac Amyloidosis (Transthyretin-Associated Familial Amyloidosis). In: Clinical Guide to Cardiovascular Disease. Springer, London. https://doi.org/10.1007/978-1-4471-7293-2_24

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  • DOI: https://doi.org/10.1007/978-1-4471-7293-2_24

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  • Publisher Name: Springer, London

  • Print ISBN: 978-1-4471-7291-8

  • Online ISBN: 978-1-4471-7293-2

  • eBook Packages: MedicineMedicine (R0)

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