Muscular Dystrophy Fact Sheet
Muscular Dystrophy Fact Sheet
Muscular Dystrophy Fact Sheet
Muscular Dystrophy is a group of genetic diseases thats characterized by progressive weakness and degeneration of voluntary skeletal muscles.
There are 9 main forms of MD. Most common kind of Muscular Dystrophy is Duchenne Muscular Dystrophy. Usually occurs 1 in every 3500 males. Becker Muscular Dystrophy is a more mild form. There are many other forms of Muscular Dystrophy that also effect females including LimbGirdle MD and Myotonic MD. It is believed more then 50,000 Americans are affected with MD.
Michelle Haddock
An inherited defective gene or a random mutation of a gene causes Muscular Dystrophy. These genes are found on the X-chromosome. The affected genes regulate proteins that aide in muscle maintenance. In Duchenne Muscular Dystrophy, it is inherited from the mother, a mutated gene on the Xchromosome, even if the mother shows no signs of DMD. Inheritance of DMD can be seen in the image on the left. There is no cure but research is promising in the areas of Stem cells, gene therapy, and exon skipping.
Resources
There are many wonderful resources that can be found at mda.org Local MDA office 6305 Ivy Lane #320 Greenbelt, MD 20770 301-486-7680 Infants and Toddlers Program 1450 Furnace Ave, Glen Burnie, Md. 21060 410-222-6911 http://www.aacps.org/itp
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It is important in the home and at school to encourage visitors and social interactions. Focusing on certain hobbies or interests, such as art, is also a great way of developing and maintaining intellectual and mental health. Job opportunities such as in an office or in computer aided design can be best but there are many options.
Related Laws
Individuals with Disabilities Act (IDEA) Americans with Disabilities Act (ADA) MD CARE Act Reauthorization (2013)
References
Emery, A. (2008). Muscular dystrophy (3rd ed.). Oxford, GBR: Oxford University Press.