Duchenne Muscular Dystrophy is a severe genetic condition that causes progressive muscle weakness and loss of mobility, primarily affecting boys. This article is a comprehensive guide designed to educate patients, families, and caregivers about the disease. It is organized into sections that begin with an overview of what Duchenne Muscular Dystrophy is, followed by its causes, inheritance patterns, and how it affects the body. The article discusses the risk factors, symptoms, and diagnosis process, offering insights into the importance of early detection. It then explores available treatment options, including medications, therapies, and emerging treatments like gene therapy, while also highlighting supportive care approaches to improve quality of life. The prognosis and daily challenges of living with the condition are addressed, providing practical advice and emotional support for families managing the disease. Each section builds on the previous one, offering a logical flow of information that moves from understanding the basics to more detailed discussions of management and care. Written in clear, straightforward language, the article ensures that complex medical concepts are accessible, making it a valuable resource for all readers seeking to understand Duchenne Muscular Dystrophy.