43K views · 139 reactions | Did you know that Duchenne muscular dystrophy (DMD) is a rare condition which affects 1 in every 3,500 – 5,000 male births worldwide? It can cause severe progressive muscle loss and is usually diagnosed between the ages of 3 and 6. This Rare Disease Day, we want to raise awareness of this condition, and the 20,000 children diagnosed with DMD globally each year! | Roche | Facebook
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43K views · 139 reactions | Did you know that Duchenne muscular dystrophy (DMD) is a rare condition which affects 1 in every 3,500 – 5,000 male births worldwide? It can cause
Roche. . Did you know that Duchenne muscular dystrophy (DMD) is a rare condition which affects 1 in every 3,500 – 5,000 male births worldwide? It can cause severe progressive muscle loss and is usually diagnosed between the ages of 3 and 6. This Rare Disease Day, we want to raise awareness of this condition, and the 20,000 children diagnosed ...
103K views2 weeks ago
Muscular Dystrophy Symptoms
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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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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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Doctors are studying a boy whose muscles are 40% larger than expected, despite normal myostatin levels. Research could lead to breakthroughs in muscular dystrophy treatment, potentially helping patients gain muscle and strength. A fascinating case! #MuscleGrowth #MedicalMystery #MuscularDystrophy #GeneticResearch #HealthScience From: The World's Strongest Toddler | Real Stories
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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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