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 co…
1.2K viewsMar 10, 2025
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Dr.Gaurav kr. Bhagat (Physio-therapist) on Instagram: "✅Duchenne muscular dystrophy (DMD) is a severe, progressive genetic muscle disorder caused by a mutation in the DMD gene, resulting in a lack of dystrophin protein. 1️⃣Cause: A mutation on the X chromosome prevents the production of dystrophin, causing muscle cells to become unstable, damaged, and eventually replaced by fat and scar tissue (fibrosis). 2️⃣Symptoms: Progressive muscle weakness starting in the legs/pelvis, leading to frequent f
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Dr.Gaurav kr. Bhagat (Physio-therapist) on Instagram: "✅Duche…
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