Clinical Research Directory
Browse clinical research sites, groups, and studies.
Molecular Analysis of Patients With Neuromuscular Disease
Sponsor: Boston Children's Hospital
Summary
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 many patients diagnosed with muscular dystrophy with no causative gene implicated in their disease. Using molecular genetics to unravel basis of these neuromuscular disorders will lead to more accurate diagnosis/prognosis of these disorders which will lead to potential therapies.
Official title: Molecular Analysis of Nucleic Acids Derived From Patients With Neuromuscular Disease and Their Family Members
Key Details
Gender
All
Age Range
1 Week - 100 Years
Study Type
OBSERVATIONAL
Enrollment
1000
Start Date
2002-01
Completion Date
2027-12-31
Last Updated
2023-04-24
Healthy Volunteers
No
Conditions
Locations (1)
Boston Children's Hospital
Boston, Massachusetts, United States