Loading...

Skip Navigation Links
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.

 

Join this Group


 

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.




Member Sign In

Remember me
Forgot Password?
Sign up now


Medwonders has 257354 Members and 444 Groups.
Last Updated - Dec 22, 2024 - Designed & Content Managed by Medindia4u.com Pvt. Ltd.
Copyright © 2024 Medindia4u.com Pvt. Ltd. All rights reserved.