Duchenne muscular dystrophy is a rare and progressive genetic condition that affects approximately one in 3,500 boys worldwide. On Duchenne Awareness Day, we are highlighting the importance of ongoing research, specialist care, and support for children living with this condition and their families. Since 2020, Save Our Sons Duchenne Foundation has been a valued partner of Sydney Children's Hospitals Foundation, helping to fund specialist roles and clinical trials that are making a meaningful imp
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Duchenne muscular dystrophy is a rare and progressive genetic condition that affects approximately one in 3,500 boys worldwide. On Duchenne Awareness Day, we are
Sydney Children's Hospitals Foundation. . Duchenne muscular dystrophy is a rare and progressive genetic condition that affects approximately one in 3,500 boys worldwide. On Duchenne Awareness Day, we are highlighting the importance of ongoing research, specialist care, and support for children living with this condition and their families ...
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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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