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The University of Pittsburgh reported the first study to achieve success with gene therapy for the treatment of congenital muscular dystrophy (CMD) in mice.

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15y ago

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How does muscular dystrophy progress?

Muscular dytrophy is not spread it is heriditary.


How does muscular dystrophy disrupt homeostasis?

The muscular Dystrophy do not maintain homeostasis.


When was Muscular Dystrophy Association created?

Muscular Dystrophy Association was created in 1950.


How often does muscular dystrophy occur?

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.


The form of muscular dystrophy in which survival is rarely beyond the late twenties?

Duchenne's muscular dystrophy


What is the most common and most severe type of muscular dystrophy in children?

Duchenne Muscular Dystrophy


What are goals of rehabilitation for someone with muscular dystrophy?

what are the goals fo rehabilitation for someone with muscular dystrophy


When was Muscular Dystrophy Family Foundation created?

Muscular Dystrophy Family Foundation was created in 1958.


When was Muscular Dystrophy Campaign Trailblazers created?

Muscular Dystrophy Campaign Trailblazers was created in 2008.


Is muscular dystrophy and duchenne muscular dystrophy the same?

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.


What is muscular dystrophy?

Muscular dystrophy (MD) is a genetic disorder that weakens the muscles that help the body move.


Who found Duchennes Muscular Dystrophy?

Duchenne muscular dystrophy was first described by the French neurologist Guillaume Duchenne in 1861. He conducted extensive studies on the disease, leading to its eponymous designation.