5 Medical Advancements to Watch for in 2025: FSHD Breakthroughs Included
Facioscapulohumeral muscular dystrophy (FSHD) is a genetic dysfunction that causes progressive muscle weak spot and losing. It’s the third most typical type of muscular dystrophy, affecting roughly 1 in 20,000 individuals worldwide. FSHD is attributable to a mutation within the D4Z4 gene, which is positioned on chromosome 4. This mutation ends in a lack of … Read more
