Muscular dystrophy is a genetic disorder characterized by progressive muscle weakness and degeneration. Duchenne muscular dystrophy DMD is the most common X linked disorder muscular dystrophy. It is caused by an absence of the protein named as dystrophin, which helps to keep muscle cells intact. In my research on this topic, I will emphasis on a complete analysis of molecular gene behind muscular dystrophy. According to a survey with few hospitals labs in my region with 40 50 patients, we had identified the ratio of around 90 of male and 10 of the female victim with the muscular dystrophy disorder. The lifespan of people having this disorder decreases unconditionally and it majorly effect the youngsters. Main concern for the treatment methodology or medical interventions are limited to treating symptoms. Nishtaa Modi "Analyze the Molecular Genetics of a Solitary Causative Genetic Material behind Muscular Dystrophy" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-2 , February 2020, URL: https://www.ijtsrd.com/papers/ijtsrd29850.pdf