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Myotonia atrophica
noun 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. Synonyms: myotonic dystrophy, myotonic muscular dystrophy, Steinert's disease.
WordNet 3.0 © 2010 Princeton University
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