Duchenne therapy may be evolving from slowing disease to reversing it—with RNA approaches offering the prospect of restoring function. Ongoing research will determine if these advances can deliver lasting, transformative recovery.
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New clinical evidence points to a potential breakthrough: a therapy that may not just slow but actually reverse muscle loss in boys with Duchenne muscular dystrophy. While existing treatments, such as corticosteroids and gene-targeted drugs, only…
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News Source: www.forbes.com
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