Late-onset Fabry Disease Revealed by Ventricular Tachycardia: A Case Report
HeartRhythm Case Reports（2021）
Abstract
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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Key words
Fabry disease,Ventricular tachycardia,Catheter ablation,Hypertrophic cardiomyopathy,Genetic,Syncope
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