For the first time in medical history, scientists have restored hearing in people born deaf by fixing a single faulty gene using viral gene therapy. By delivering a healthy copy of the gene directly into the inner ear, they enabled cells to create the missing protein that converts sound into electrical signals for the brain.
Children who had only known silence are now hearing voices, music, and everyday sounds for the very first time. Early clinical trials showed astonishing results, with some children beginning to recognize speech and even develop language skills within just a few months.
This groundbreaking success not only transforms lives but also highlights the enormous potential of gene therapy to tackle other inherited conditions. Experts believe this could be the beginning of a future where hereditary deafness is no longer permanent — but completely curable.
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