Children were born with serious retinal disease because they were almost blind. This disease is caused by a defective AIPL1 genome that does not allow the eye to transform the light into understandable signals by the brain. Treatment consisted of direct inserting a healthy version of this gene into the retina.
Four weeks after surgery, children’s vision, light monitoring, moving objects and navigation along the corridor were controlled using exercises. They all showed a significant improvement. The first four children were operated on one eye, while the eyes treated over time moved to the discharge of those with visually impaired from the blind category, and their ridiculous eyes remained at the same level. After that, seven children received the treatment of both eyes with more promising early results.
Experts say that this breakthrough can change the treatment of hereditary blindness.
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Source: Ferra
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