Becker muscular dystrophy

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Related to Becker muscular dystrophy: distal muscular dystrophy
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  • noun

Words related to Becker muscular dystrophy

a form of muscular dystrophy that sets in in adolescence or adulthood and progresses slowly but will affect all voluntary muscles

References in periodicals archive ?
Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
The study is open to adult males 18 - 55 who have Becker muscular dystrophy as well as adult males who don't have it.
Molecular genetic analysis of 67 patients with Duchenne/ Becker muscular dystrophy.
The patient was a 40-year-old male in whom Becker muscular dystrophy (BMD) had been diagnosed clinically, bioptically, and genetically 11 years before.
Other, less severe forms of muscular dystrophy include Becker muscular dystrophy (BMD), Emery-Dreifuss muscular dystrophy (EDMD), facioscapulohumeral muscular dystrophy (FMD), limb-girdle muscular dystrophy (LGMD) and myotonic dystrophy (MMD).
The muscle cell lines will display the genes for Duchenne muscular dystrophy, Emery-Dreifuss muscular dystrophy, spinal muscular atrophy Type I, facioscapulohumeral muscular dystrophy 1A, and Becker muscular dystrophy.
Have a confirmed diagnosis or be suspected of having Duchenne or Becker muscular dystrophy based on clinical symptoms, as assessed by their treating physician, and have a positive creatine kinase (CK) test.
In a clinical trial, tadalafil--commonly known by brand names Cialis and Adcirca--reversed the effects of a biochemical chain of events that, in Becker muscular dystrophy, deprives muscles of an important chemical, nitric oxide, which normally tells blood vessels to relax during exercise, increasing blood flow and oxygenation.
PTC recently launched a global, registration-directed Phase 2b trial in DMD and Becker muscular dystrophy (BMD) to evaluate the efficacy of PTC124 as measured by improvements in the walking ability of patients with this progressive genetic disease.
Steve Higginson, 49, from Colwyn Bay, has struggled to find appropriate care for his Becker muscular dystrophy for many years.
Genes frequently involved in complex GKD include DMD, variations in which cause Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), and NR0B1 (DAX1), which is responsible for adrenal hypoplasia congenita (AHC) (2, 3).
para]]Frontier Pharma: Duchenne Muscular Dystrophy and Becker Muscular Dystrophy - Identifying and Commercializing First-in-Class Innovation[[/para]]