Closing in on a cure for Duchenne muscular dystrophy | Brain | Discovery | UT Southwestern Medical Center
utswmed.org
Closing in on a cure for Duchenne muscular dystrophy | Brain | Discovery | UT Southwestern Medical Center
Using an advanced gene editing technology called CRISPR, our team of scientists at UT Southwestern has been able to stop the progression of Duchenne muscular dystrophy in animals and human cells – a breakthrough that could ultimately change the prognosis for the most common fatal genetic disease in boys.
Jan 25, 2021
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Most boys with Duchenne muscular dystrophy don’t live past their early teens. There’s no cure and about 1 in every 3,500 to 5,000 boys are born with it. But here he is at 22 years old, still defying every odd. 💜 Every day is a blessing, and every smile is a reminder of God’s grace. 🙏🏾 #DuchenneAwareness #CaregiverJourney #FaithOverFear #EveryDayABlessing #UnbreakableSpirit #CaregiverLife #LoveInAction #FaithAndStrength #CaregiversHeart #LifeIsAGift #GodsPlan #ResilientSpirit #FamilyBond #Grat
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Most boys with Duchenne muscular dystrophy don’t live past their early teens.
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