Medics at Moorfields Eye Hospital in London have pioneered a groundbreaking gene therapy that has restored sight in young children with a rare genetic condition, preventing blindness. The therapy involved injecting healthy copies of the affected gene, allowing previously blind children to see shapes, recognize faces, and even read. Parents expressed profound amazement at their children's rapid improvement in vision, illustrating the therapy's transformative potential. Medical professionals are hopeful that further trials will lead to broader licensing of this innovative treatment across the UK and beyond.
The pioneering gene therapy administered at Moorfields Eye Hospital has proven life-changing for children born blind due to a rare genetic condition.
Patients who underwent the therapy can not only see shapes and identify toys but can even read and write, marking a significant advancement in treatment.
Jace's mother shared how his ability to track objects improved drastically; post-surgery, he is now actively engaging with his surroundings, showcasing significant visual development.
Specialists express hope for the gene therapy's wider availability, aiming to license it as a standard treatment in the UK and potentially abroad.
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