Molecular Analysis of Patients With Neuromuscular Disease
Recruiting
Observational Study
Neuromuscular; Disorder, Hereditary
Duchenne/Becker Muscular Dystrophy
Limb-girdle Muscular Dystrophy
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 1 Week – 100
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,000 (estimated)
- Sponsor
- Boston Children's Hospital · Other
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About This Trial
The purpose of this study is to identify new genes responsible for neuromuscular disorders and study muscle tissue of patient with known neuromuscular disease, as well as their family members. We are interested in recruiting many types of neuromuscular disease including; Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and limb-girdle muscle dystrophy (LGMD). There are still man…
Trial Locations
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Eligibility Criteria
The samples used in this study will be derived from individuals at risk for, or suffering from, neuromuscular disease, generally resulting in clinical weakness of one or more muscle groups and their family members.
Inclusion criteria:
1. having a clinical and/or pathological diagnosis of a muscula…
Contacts