Muscular dystrophy (MD) encompasses a group of genetic disorders that lead to progressive muscle weakness and degeneration. The most common form, Duchenne muscular dystrophy (DMD), affects approximately 1 in 3,500 male births. Other types of muscular dystrophy have varying prevalence rates, but overall, MD collectively affects about 1 in 5,000 to 1 in 10,000 individuals. The exact frequency can vary based on the specific type and population studied.
Yes, hypotonia can be related to muscular dystrophy. Muscular dystrophy encompasses a group of genetic disorders characterized by progressive muscle weakness and degeneration, often leading to hypotonia, especially in young children. The degree of hypotonia may vary depending on the specific type of muscular dystrophy and its progression. However, hypotonia can also result from other conditions unrelated to muscular dystrophy.
Muscular dytrophy is not spread it is heriditary.
The muscular Dystrophy do not maintain homeostasis.
Muscular Dystrophy Association was created in 1950.
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Muscular dystrophy is a group of genetic disorders characterized by muscle weakening and wasting, while Duchenne muscular dystrophy (DMD) is a specific type of muscular dystrophy caused by mutations in the dystrophin gene. DMD is the most common and severe form of muscular dystrophy, typically affecting boys and leading to progressive muscle weakness and loss of function.
Duchenne's muscular dystrophy
Duchenne Muscular Dystrophy
what are the goals fo rehabilitation for someone with muscular dystrophy
Muscular Dystrophy Campaign Trailblazers was created in 2008.
Muscular Dystrophy Family Foundation was created in 1958.
Muscular dystrophy (MD) is a genetic disorder that weakens the muscles that help the body move.