馃敩 After decades of research, the FDA has approved the first-ever gene therapy for Duchesne muscular dystrophy, developed at Nationwide Children's Hospital.
馃拤 Dr. Jerry Mendel, who launched the gene therapy research project in 1999, calls the newly approved therapy the biggest event in the history of muscular dystrophy.
馃懄 The gene therapy offers hope for restoring movement and motion in children with Duchesne muscular dystrophy, improving their quality of life.
馃彞 Ohio medical team makes breakthrough in muscular dystrophy treatment.
馃К Muscular dystrophy is a genetic disorder that progressively weakens muscles.
馃挕 Dr. Men's treatment involves using a virus as a delivery system.
馃挕 An Ohio medical team has made a breakthrough in treating muscular dystrophy using viral genes injected into the veins of children to replace disease genes and restore muscle function.
馃檶 The FDA has approved this treatment, leading to emotional reactions from the medical team and positive impact on young lives.
馃挭 Dr. Mandel and nurse practitioner Kelly Layman collaborate to implement the treatment, with Layman taking care of practical tasks and Dr. Mandel taking on the role of the 'good guy'.
馃彞 Ohio medical team achieves breakthrough in muscular dystrophy treatment.
馃挐 Patients express gratitude to Dr. Mendel for the successful gene therapy treatment.
馃敎 Serepta Therapeutics plans to make the treatment widely accessible in the near future.
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