RECRUITINGOBSERVATIONAL
A Registered Cohort Study on Duchenne Muscular Dystrophy
About This Trial
Dystrophinopathy is a term of X-linked recessive genetic disease, including Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and the X-linked dilated cardiomyopathy. The aim of this study is to determine the clinical spectrum and natural progression of dystrophinopathy in a prospective multicenter natural history study, to assess the clinical, genetic of patients with dystrophinopathy to optimize clinical management.
Who May Be Eligible (Plain English)
Who May Qualify:
- Beyond 2 years old
- Diagnosis with Duchenne Muscular Dystrophy, and female carriers, genotypically confirmed
- Diagnosis should be supported by muscle biopsy, if no genetic confirmation.
Who Should NOT Join This Trial:
- Presence of other clinically significant illness
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Beyond 2 years old
* Diagnosis with Duchenne Muscular Dystrophy, and female carriers, genotypically confirmed
* Diagnosis should be supported by muscle biopsy, if no genetic confirmation.
Exclusion Criteria:
* Presence of other clinically significant illness
Locations (1)
First Affiliated Hospital of Fujian Medical University
Fuzhou, China