Duchenne and Becker muscular dystrophy are genetic disorders characterized by progressive muscle weakness due to the absence or deficiency of a protein called dystrophin. Duchenne muscular dystrophy (DMD) is more severe and begins in early childhood, while Becker muscular dystrophy (BMD) is milder and progresses more slowly, often appearing in adolescence or early adulthood. These conditions primarily affect boys and gradually impact mobility, muscle strength, and eventually heart and respiratory function. Early diagnosis and supportive care can help improve quality of life and slow disease progression.