[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]

MeSH terms

• Adolescent
• Child
• Child, Preschool
• Chromosome Deletion*
• Dystrophin / genetics*
• Humans
• Infant
• Infant, Newborn
• Muscle Hypotonia / diagnosis
• Muscle Hypotonia / genetics
• Muscular Dystrophies / diagnosis*
• Muscular Dystrophies / genetics
• Mutation / genetics*
• Myoglobinuria / diagnosis
• Myoglobinuria / genetics