Abstract Fabry disease is a metabolic alteration linked to an enzymatic deficiency of Alpha-Galactosidase A. this disorder compromises the sphingolipid metabolism. leading to an accumulation of lysosomal globotriaosylceramide and is inherited in an X-linked recessive way. The diagnostic of this disease. https://atome3des.shop/product-category/graveur-decoupeur-laser/