Condition 1: Dystrophinopathy(Duchenne muscular dystrophy, Becker muscular dystrophy). Condition 2: Spinal muscular atrophy. Condition 3: other Myopathy (Congenital myopathy, Congenital myasthenic syndrome). Condition 4: Charcot-Marie-Tooth). Muscular dystrophy Spinal muscular atrophy and related syndromes Congenital myopathies Hereditary motor and sensory neuropathy
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Genetic confirmed patients with Dystrophinopathy(Duchenne muscular dystrophy, Becker muscular dystrophy) Genetic confirmed patients with Neuropathy(Spinal muscular atrophy, Charcot-Marie-Tooth) Genetic confirmed patients with other Muscular dystrophy(Limb girdle muscular dystrophy, Congenital muscular dystrophy) Genetic confirmed patients with other Myopathy (Congenital myopathy, Congenital myasthenic syndrome)
Exclusion criteria
Exclusion criteria: Patients with cancer Patients with chromosomal defects Patients with HIV, HCV, HBV, HTLV1,2 Dissatisfaction for entering the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Muscle power. Timepoint: Before study, 6 and 9 and 12 months after Mesenchymal stem cell transplantation. Method of measurement: Walking distance in 6 minutes and muscular force examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran Islamic Azad university of Medical Sciences