Exploring Muscular Dystrophies

This chapter provides a comprehensive overview of various muscular dystrophies, focusing primarily on Duchenne and Becker muscular dystrophies, including their characteristics, progression, and treatment options. It highlights the importance of diagnostic tools such as dystrophin staining and discusses other neuromuscular disorders like facioscapulohumeral and myotonic dystrophies. Key clinical features, genetic causes, and potential complications are analyzed to aid in early identification and management of these conditions.