New gene therapy for Duchenne muscular dystrophy offers hope - UW Medicine | Newsroom
New gene therapy for Duchenne muscular dystrophy offers hope - …
Jul 22, 2024
uw.edu
Closing in on a cure for Duchenne muscular dystrophy | Brain | Discovery | UT Southwestern Medical Center
Closing in on a cure for Duchenne muscular dystrophy | Brain | Disc…
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utswmed.org
Tucson child receives first gene therapy treatment for Duchenne muscular dystrophy.
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YouTubeCureDuchenneMD
Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
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Reviewing the Treatment Landscape for Duchenne Muscular Dystrophy
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