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Duchenne muscular dystrophy

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noun Du·chenne muscular dystrophy \dü-ˈshen-, də-\

Definition of Duchenne muscular dystrophy

  1. :  a severe progressive X-linked muscular dystrophy of males marked by early childhood onset and absence of the protein dystrophin —called also Duchenne's muscular dystrophy — compare becker muscular dystrophy



Origin of duchenne muscular dystrophy

Guillaume Armand Duchenne †1875 French neurologist


First Known Use: 1971


Medical Dictionary

Duchenne muscular dystrophy

noun Du·chenne muscular dystrophy

Medical Definition of Duchenne muscular dystrophy

  1. :  a severe progressive form of muscular dystrophy of males that appears in early childhood, affects the muscles of the legs before those of the arms and the proximal muscles of the limbs before the distal ones, is inherited as an X-linked recessive trait, is characterized by complete absence of the protein dystrophin, and usually has a fatal outcome by age 20—abbreviation DMD; see becker muscular dystrophy



Variants of duchenne muscular dystrophy

also Duchenne's muscular dystrophy

Learn More about duchenne muscular dystrophy


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