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  • Myotonic Dystrophy (DM) - Diseases | Muscular Dystrophy Association
    What is myotonic dystrophy (DM)? Myotonic dystrophy (DM) is a form of muscular dystrophy that affects muscles and many other organs in the body The word “myotonic” is the adjectival form of the word “myotonia,” defined as an inability to relax muscles at will The term “muscular dystrophy” means progressive muscle degeneration, with weakness and shrinkage of the muscle tissue
  • Myotonic Dystrophy (DM) - Muscular Dystrophy Association
    MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases
  • Types of Myotonic Dystrophy (DM) - Diseases | Muscular Dystrophy . . .
    Myotonic Dystrophy (DM) Types of Myotonic Dystrophy Myotonic dystrophy (DM) includes two major types — DM1 and DM2 — both caused by genetic defects They result in multisystem disorders characterized by skeletal muscle weakness and myotonia (difficulty relaxing muscles after use), cardiac abnormalities, cataracts, and other abnormalities
  • Myotonic Dystrophy
    Myotonic Dystrophy Myotonic dystrophy (DM) is a musculoskeletal disorder that affects the muscles and a number of different organs in the body DM is the most common form of muscular dystrophy that begins in adulthood, usually in the 20s or 30s It is a genetic disorder characterized by progressive muscle loss and weakness
  • Myotonic Dystrophy (DM) - Muscular Dystrophy Association
    Medical management This section addresses medical management of the many symptoms of adult-onset DM1 and DM2, as well as childhood-onset DM1 These three forms of DM share similar medical management strategies Multidisciplinary surveillance and management of these and other issues is optimal Recommendations regarding management are based more on consensus and clinical experience than on
  • Causes Inheritance - Myotonic Dystrophy (DM) - Diseases | Muscular . . .
    What causes DM? Type 1 myotonic dystrophy (DM1) and type 2 myotonic dystrophy (DM2) are both caused by abnormally expanded stretches of DNA The expansions occur in two different genes but appear to have similar effects on various cells, particularly the cells of the voluntary and involuntary muscles, including the heart and nervous system DM provides an example of mechanism of disease called
  • What Myotonic - Muscular Dystrophy Association
    Dystrophy Myotonic dystrophy (DM) is a musculoskeletal disorder that affects the muscles and a number of different organs in the body DM is the most common form of muscular dystrophy that begins in adulthood, usually in the 20s or 30s It is a genetic disorder characterized by progressive muscle loss and weakness
  • Medical Management - Myotonic Dystrophy (DM) - Diseases | Muscular . . .
    Myotonic Dystrophy (DM) Medical Management As yet, there is not a specific treatment that “gets at the root” of type 1 or type 2 myotonic dystrophy (DM1, DM2) Treatment is aimed at managing symptoms and minimizing disability This section first addresses medical management of the many symptoms of adult-onset DM1 DM2 and childhood-onset DM1
  • Muscular Dystrophy Association
    Muscular Dystrophy Association (MDA) has been at the center of progress for people living with muscular dystrophy, ALS, and over 300 other neuromuscular conditions for 75 years





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