Search Results 1-10 of 26680 for Duchenne+muscular+dystrophy
ANSWER: As with all forms of muscular dystrophy, Duchenne muscular dystrophy is caused by a genetic defect. The defect leads to muscle weakness and loss of ...
Muscle pain and stiffness; Learning disabilities; Delayed growth. Becker muscular dystrophy. Signs and symptoms are similar to those of Duchenne muscular ...
In 2019, the Food and Drug Administration (FDA) approved golodirsen (Vyondys 53) for treatment of some people with Duchenne dystrophy who have a certain genetic ...
Viltolarsen injection is used to treat Duchenne muscular dystrophy (DMD) in patients with a confirmed specific genetic mutation. DMD is a rare, inherited muscle ...
In 2019, the FDA approved golodirsen (Vyondys 53) for treatment of some people with Duchenne dystrophy who have a certain genetic mutation. Heart medications, ...
Deflazacort is used to treat Duchenne muscular dystrophy (DMD). DMD is a rare, inherited muscle disease that occurs usually in children and young adults and ...
About this study. The expanded access program will provide access to treatment with deflazacort in children, adolescent, and adult patients with DMD in the ...
Vamorolone is used to treat Duchenne muscular dystrophy (DMD). DMD is a rare, inherited muscle disease that is caused by absence of a protein called ...
... Duchenne muscular dystrophy, Degenerative disk disease, Cervical spondylotic myelopathy, Arthropathy, Inflammatory arthritis, Radiculopathy, Muscle weakness ...
Golodirsen injection is used to treat Duchenne muscular dystrophy (DMD) in patients with a confirmed specific genetic mutation. DMD is a rare, inherited muscle ...
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