Duchenne muscular dystrophy (DMD) is the commonest inherited neuromuscular disorder of
childhood and mainly affects males. Over the course of the last century, the average life …

Duchenne muscular dystrophy (DMD) is a severe and fatal muscle condition affecting young
children. Without interventions, affected boys lose the ability to walk independently by the …

Duchenne muscular dystrophy (DMD) is familiar to paediatricians as the most common
childhood muscular dystrophy and leads to severe disability and early death in the late …

Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of
childhood for which there is no cure. This authoritative guide provides a clear overview of …

Duchenne muscular dystrophy (DMD) is the most common and severe childhood muscular
dystrophy, resulting in progressive muscle weakness and wasting, disability and decreased …

Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy in
childhood. It is caused by mutations of the DMD gene, leading to progressive muscle …

Abstract Duchenne Muscular Dystrophy (DMD) is an X-linked recessive disorder caused by
a deficient or defective synthesis of dystrophin protein. DMD is the most common form of …

Duchenne muscular dystrophy (DMD), an inherited X-linked recessive disorder, is
characterized by progressive symmetric muscle weakness and gait disturbance, with onset …

Duchenne muscular dystrophy is the most common form of childhood muscular dystrophy. A
mutation in the DMD gene disrupts dystrophin (protein) production, causing damage to …

Duchenne muscular dystrophy (DMD) is the commonest and best-known of the muscular
dystrophies. Being an X-linked disorder, it affects mainly boys. The disease gene was …