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1. A severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
   - myotonic muscular dystrophy, myotonia atrophica, Steinert's disease

Derived forms: myotonic dystrophies

Type of: dystrophy, muscular dystrophy

Encyclopedia: Myotonic dystrophy