There is so far no treatment to cure FD, but only supportive enzyme replacement therapies (ERTs) involving infusions of recombinant human α-Gal A (rhα-GLA), commercially named Fabrazyme (Agalsidase beta) and Replagal (Agalsidase alfa), to consistently stabilize patients’ kidney function, decrease neuropathic pain, and reverse or improve hypertrophic cardiomyopathy [4,5]. Here, GLA is linked to Fabry disease.