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Genetic and Metabolic :
Muscular Dystrophy / Duchenne Muscular Dystrophy

Muscular dystrophy (MD) refers to a group of hereditary disorders which causes muscles to weaken and waste away. There is no cure for MC, but drug treatment for symptoms, therapy, and assistive technology can make a huge difference for a person with the condition.

Learn more about muscular dystrophy from doctors and other people and families dealing with the condition in this online support group for MD.

 

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1. Which doctor should be consulted if there is a patient of Muscular dystrophy?

A child specialist should first be consulted, however for long term management many a team of doctors including physiotherapist, chest specialist, orthopedicians are required.

2. What is the prognosis of DMD?

DMD is a progressive disorder and the patient usually dies before age 25.

3. Can DMD be prevented?

DMD is a genetic disorder. There are no tests to detect DMD in a child before birth. However, genetic counseling helps in the identification of at risk families.

4. When does a doctor suspect Duchenne Dystrophy (DMD)?

DMD is suspected when boys present with walking difficulties usually around the age of 2 or 3 years.




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