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Duchenne's muscular dystrophy

   Also found in: Medical, Encyclopedia, Wikipedia 0.01 sec.
Du·chenne's muscular dystrophy  (d-shnz)
n.
The most common form of muscular dystrophy, in which fat and fibrous tissue infiltrate muscle tissue, causing eventual weakening of the respiratory muscles and the myocardium. The disease, which almost exclusively affects males, begins in early childhood and usually causes death before adulthood.

[After Guillaume B.A. Duchenne (1806-1875), French physician.]
ThesaurusLegend:  Synonyms Related Words Antonyms
Noun1.Duchenne's muscular dystrophy - the most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males)
dystrophy, muscular dystrophy - any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles


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Scientists now know that people with Duchenne's muscular dystrophy have a defective gene that causes the devastating muscle weakness.
But in April, he began wiggling the four biggest toes of his left foot more vigorously, giving new hope to the boy and thousands like him with Duchenne's muscular dystrophy, a genetic disease characterized by defective muscle cells that cannot produce a protein called dystrophin (SN: 1/2/88, p.
CepTor's primary efforts are currently being focused on moving its lead product, MYODUR, into phase I/II clinical trials for Duchenne's muscular dystrophy.
 
 
 
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