Muscular dystrophy (MD) encompasses a heterogeneous group of genetic disorders characterized by progressive muscle weakness and degeneration. Its etiology lies in mutations affecting genes responsible for the structure and function of muscle fibers, resulting in impaired muscle integrity and function. The severity and progression of the disease vary widely among individuals, depending on the specific genetic mutation and subtype of muscular dystrophy. This course will provide a detailed examination of the types of muscular dystrophy, including Duchenne, Becker, Limb-Girdle, Facioscapulohumeral, and Myotonic dystrophies, among others. Each subtype exhibits distinct patterns of inheritance, clinical manifestations, and affected muscle groups, raising the need for tailored approaches to assessment and intervention. The course will also cover diagnoses, treatment, plans of care, mobility challenges, systems affected, and the impact on daily life. By the end of the course, Physical Therapists and Physical Therapist Assistants will be equipped with the knowledge and skills to develop comprehensive plans of care for individuals with muscular dystrophy tailored to their unique needs, goals, and disease progression.