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A novel genotype–phenotype overlap: transthyretin cardiac amyloidosis with a pathogenic CTNNA3 truncating variant presenting with malignant ventricular arrhythmias

2026-06-16

Abstract excerpt

<title>Abstract</title> <p>Background: Transthyretin cardiac amyloidosis (ATTR-CM) may mimic hypertrophic cardiomyopathy and, in rare cases, coexist with genetic cardiomyopathies, potentially increasing arrhythmic risk. <h4>Methods:</h4> An 82-year-old man with atrial fibrillation presenting with progressive heart failure symptoms underwent comprehensive clinical, electrocardiographic, echocardiographic, hematol...

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Literature Corpus work
652064f4-f197-509f-befe-ec8c10195e01
DOI
10.21203/rs.3.rs-9658027/v1
Open publication

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A novel genotype–phenotype overlap: transthyretin cardiac amyloidosis with a pathogenic CTNNA3 truncating variant presenting with malignant ventricular arrhythmiasDOI 10.21203/rs.3.rs-9658027/v1
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