Duchenne and Becker muscular dystrophies are both genetic disorders that affect the muscles. Duchenne muscular dystrophy is the more severe form, typically diagnosed in early childhood, while Becker muscular dystrophy is a milder form that may not be diagnosed until later in life. Research in this area focuses on understanding the genetic mutations that cause these disorders, as well as developing treatments to slow the progression of muscle weakness and improve quality of life for affected individuals. Current research also includes investigating gene therapy and other potential treatments to address the underlying causes of these diseases. Early diagnosis and treatment interventions are crucial in managing these conditions and improving outcomes for patients.