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16-year-old Jonathan Lubin, with sickle cell disease, underwent experimental CRISPR gene editing therapy, reducing pain crises and hospitalizations.
Sixteen-year-old Jonathan Lubin is a sickle cell disease patient who received experimental CRISPR gene editing therapy at New York-Presbyterian/Columbia.
The treatment required chemotherapy and involved the complex process of harvesting, editing, and reintroducing his own stem cells.
Today, Lubin has not experienced a pain crisis or hospitalization for over two years, reflecting a stark contrast to his previous life filled with frequent hospital visits.
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Jonathan Lubin, de 16 años, con anemia falciforme, se sometió a una terapia experimental de edición genética CRISPR, que redujo las crisis de dolor y las hospitalizaciones.