Search Results 1-10 of 27406 for Duchenne+muscular+dystrophy
Muscular dystrophy is an umbrella term applied to a group of muscle diseases in which there is a known genetic abnormality that affects proteins needed to form ...
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 ...
About this study. The expanded access program will provide access to treatment with deflazacort in children, adolescent, and adult patients with DMD in the ...
... Duchenne muscular dystrophy (DMD) in patients with a confirmed specific genetic mutation. DMD is a rare, inherited muscle disease that is caused by absence ...
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 ...
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 ...
Eteplirsen injection is used to treat Duchenne muscular dystrophy (DMD) in patients with a confirmed mutation of the dystrophin gene amenable to exon 51 ...
... Duchenne muscular dystrophy, Degenerative disk disease, Cervical spondylotic myelopathy, Arthropathy, Inflammatory arthritis, Radiculopathy, Muscle weakness ...
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