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A Canadian success story: world-first to treat Fabry disease with gene therapy

 E-Mail IMAGE: Darren Bidulka rests after his modified blood stem cells were transplanted into him at the Foothills Medical Centre in Calgary in 2017, allowing him to stop his enzyme therapy. (From. view more  Credit: Courtesy of Darren Bidulka (Thursday, Feb. 25, 2021, Toronto) Results of a world-first Canadian pilot study on patients treated with gene therapy for Fabry disease show that the treatment is working and safe. The Canadian research team was the first to use gene therapy in 2017 to treat patients with Fabry disease, a rare, chronic illness that can damage major organs and shorten lives. They report their findings today in the journal

A Canadian success story: world-first to treat Fabry disease with gene therapy

A Canadian success story: world-first to treat Fabry disease with gene therapy
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