Revised and Updated CMD GeneReview Overview Chapter released!

Thanks to Dr. Susan Sparks, Dr. Susana Quijano Roy and Dr. Amy Harper and the GeneReview editorial staff fot their tremendous work in revising and updating the CMD Overview Chapter, which provides current information on how to diagnose and manage CMD.   Next stop: revision of the Laminin Alpha 2 Deficient (Merosin Def) CMD.
To read chapter

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  • Congenital Muscular Dystrophy

    A group of diseases causing muscle weakness at birth. Several defined genetic mutations cause muscles to break down faster than they can repair or grow. A child with CMD may have various neurological or physical impairments. Some children never gain the ability to walk, while others lose the ability as they grow older. Learn more...

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