Late-onset Fabry Disease Revealed by Ventricular Tachycardia: A Case Report

Geoffroy Ditac,Kévin Gardey,Antoine Jobbé-Duval,Alain Fouilhoux,Gilles Millat,Philippe Chevalier

HeartRhythm Case Reports（2021）

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摘要

Fabry disease (FD) is an X-linked lysosomal storage disorder due to mutations in the GLA gene leading to deficiency of lysosomal α-galactosidase A (α-Gal A). Classic FD causes multiorgan failure, whereas the later-onset phenotype is characterized by predominantly cardiac manifestations. Ventricular arrhythmias are among the complications.1,2

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关键词

Fabry disease,Ventricular tachycardia,Catheter ablation,Hypertrophic cardiomyopathy,Genetic,Syncope

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