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.
Study Type
OBSERVATIONAL
Enrollment
2,000
First Affiliated Hospital of Fujian Medical University
Fuzhou, China
RECRUITINGAge at death
the time when patient die
Time frame: 20 years
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