Ventricular Tachycardia Revealing an Anderson– Fabry Disease: A Rare Case Report
Charif H., B. E. Ovaga, Jama D., P. Mulendele, Njie M., Haboub M., Arous S., Bennouna E. M., Drighil A. & Habbal R. · Asian Journal of Research in Cardiovascular Diseases · 2023
Anderson-Fabry disease ranks as the second most common lysosomal storage disorder. It is a hereditary and rare metabolic condition resulting from a mutation in the GLA gene, responsible for encoding the lysosomal enzyme alpha-galactosidase A. This condition impacts multiple organ...
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Research Article