Duchenne Muscular Dystrophy: Public Education

Abstract

Duchenne Muscular Dystrophy (DMD) is a severe genetic disorder that affects the muscles, causing them to weaken over time. This condition primarily impacts boys and leads to progressive physical disability, requiring comprehensive care and management. This guide provides an accessible yet detailed explanation of DMD, addressing its causes, inheritance patterns, symptoms, diagnosis, treatment, and daily management. The content is designed to serve as a valuable resource for patients, families, and caregivers seeking clarity on this condition. Understanding the role of the dystrophin gene and exploring treatment options, including emerging therapies, is critical to managing DMD and improving the quality of life for those affected.