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Fabry Disease Pipeline Market — Gene Therapy, Next-Generation ERT, and the Race to Transform Rare Disease Treatment
Fabry disease — an X-linked lysosomal storage disorder caused by mutations in the GLA gene encoding alpha-galactosidase A (alpha-Gal A) — is a progressive multisystem condition affecting the heart, kidneys, nervous system, and skin through accumulation of globotriaosylceramide (Gb3) in cells throughout the body. With an estimated prevalence of approximately 1 in 40,000–100,000...
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