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London doctors improve vision in four children with rare blindness through new gene therapy.
Doctors in London have successfully treated four young children with a rare form of blindness called Leber Congenital Amaurosis (LCA) using a pioneering gene therapy.
The treatment involves injecting healthy copies of the AIPL1 gene into the retina, which significantly improved the children's vision, enabling them to see shapes and even read and write.
This groundbreaking therapy offers hope for other children with genetic blindness.
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Los médicos de Londres mejoran la visión en cuatro niños con ceguera rara a través de una nueva terapia genética.