Myotonic Dystrophy Type 1: Mechanism of Disease
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YouTubeThe France Foundation
Myotonic Dystrophy Type 1: Mechanism of Disease
Learn about the mechanism of disease for Myotonic Dystrophy Type 1 (DM1). Watch this short animation to discover what causes this rare genetic disorder. For CME information, please visit: https://www.francefoundation.com/9380-dm1-explore-cme This content is intended for neurologists, physical therapists and physiatrists, cardiologists ...
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Myotonic dystrophy type 1 (DM1) is a complex, multisystem disease, affecting all systems in the body, including muscle, respiratory, cardiac, gastrointestinal and cognitive function. As we approach International Myotonic Dystrophy Awareness Day on September 15, we’re thankful to Sarah and the DM1 community for sharing their stories. Below, hear Sarah share how DM1 affects her daily life and stay tuned for the full video on September 15th to learn more about her journey. | Dyne Therapeutics
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Myotonic dystrophy is an autosomal dominant genetic disorder that can be broken down into: type 1, which is caused by the expansion of more than 50 CTG trinucleotide repeats in the DMPK gene, has a congenital and an adult form and is more severe; and type 2, which is caused by the expansion of more than 75 CCTG tetranucleotide repeats in the CNBP gene, is adult-onset and milder. To learn more, watch our video: http://osms.it/myoto8c5a5 #FOAMed #learnmedicine #Osmosis #boardreview #medicine #path
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