Duchenne Muscular Dystrophy (DMD) is a devastating genetic disorder that progressively weakens the muscles of children, predominantly boys, due to mutations in the dystrophin gene. Despite medical advancements, there is currently no definitive cure for DMD. However, regenerative medicine has opened new avenues of treatment particularly the use of Umbilical Cord-Derived Mesenchymal Stem Cells (UC-MSC Stem Cells). […]
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