Published Paper Details:

-Congenital Muscular Dystrophy (CMD) is one of the variants of muscle weakness disorders presenting early in life during infancy and soon after birth, most of these disorders are inherited and linked to specific genes.[1] The global prevalence of muscular dystrophy is 3.6 per 100,000 people.[2] CMDs are characterized by hypotonia, muscle weakness, and delays in achieving motor milestones.[3] There is no exact correlation for this disease in Ayurveda, however, it could be understood as Adibalapravrutta mamsadhatugata vatavyadhi (hereditary anomalies affecting muscle tissues due to vitiated Vata) Guidelines for the multidisciplinary care for Duchenne muscular dystrophy that address obtaining a genetic diagnosis and managing the various aspects of the disease have been established. In addition, a number of therapies that aim to restore the missing dystrophin protein or address secondary pathology have received regulatory approval and many others are in clinical development