Duchenne and Becker muscular dystrophy registry
Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.
This registry collects information about people with Duchenne or Becker muscular dystrophy, including women who carry the gene (with or without symptoms). It may help researchers better understand the condition and plan future studies.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have Duchenne muscular dystrophy or Becker muscular dystrophy, or you are a female genetic carrier.
- If you are a female carrier, you can participate even if you don’t have symptoms.
- Your diagnosis must be Duchenne or Becker muscular dystrophy.
- You must not have another type of muscular dystrophy (such as limb-girdle muscular dystrophy).
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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