BMD

(redirected from Becker muscular dystrophy)
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Related to Becker muscular dystrophy: distal muscular dystrophy
References in periodicals archive ?
Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.
Summary Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are rare progressive muscle wasting disorders.
Carriers of Duchenne and Becker muscular dystrophy (DMD and BMD, respectively) are at risk for cardiac disease.
DALLAS, April 16, 2015 /PRNewswire-iReach/ -- Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are rare progressive muscle wasting disorders.
Carrier screening for Duchenne and Becker muscular dystrophy and spinal muscular atrophy, in which deletions are frequent and for which quantitative assays have already been developed (18-21), should benefit from this technical improvement.
Parent Project Muscular Dystrophy (PPMD) is a national not-for-profit organization founded in 1994 by parents of children with Duchenne and Becker muscular dystrophy.
This six patient clinical trial follows from a trial of the therapy in Becker muscular dystrophy patients that demonstrated initial safety and efficacy.
Duchenne and Becker muscular dystrophy (DMD/BMD) are X-linked allelic neuromuscular defects caused by mutations in the dystrophin gene, which spans 2.