Duchenne muscular dystrophy (DMD) is inherited as an X-linked recessive disorder which
affects 1 in 3600 to 6000 live male births and is the most common childhood neuromuscular …

Duchenne muscular dystrophy (DMD) is the most common childhood muscular dystrophy,
affecting 1 in 3500 live male births. Mutations in the X chromosome result in an absence of …

Dystrophinopathies are a group of X-linked neuromuscular disorders arising from mutations
in the dystrophin (DMD) gene. The DMD gene encodes dystrophin protein, which plays an …

Duchenne muscular dystrophy (DMD) is an X-linked genetic disorder that causes
progressive weakness and wasting of skeletal muscular and myocardium in boys due to …

Duchenne muscular dystrophy (DMD) is a genetic disorder that presents with progressive
muscle degeneration and weakness. It is caused by alteration of a protein called dystrophin …

After advances in clinical care and newer efforts in therapeutic approaches, life span has
lengthened in Duchenne muscular dystrophy (DMD). Starting from eary 1980s, each decade …

Duchenne muscular dystrophy (DMD), an X-linked disorder, is the most common muscular
dystrophy in children, presenting in early childhood and characterized by proximal muscle …

Duchenne muscular dystrophy (DMD) is an X-linked, severe genetic muscular disorder
caused by the deficiency of DMD gene. There is still no curative therapy for the disease, but …

Duchenne muscular dystrophy is a genetic orphan neuromuscular disease caused by a
mutation in the DMD gene encod‑ing the protein dystrophin. As a result of developing and …

Abstract Background Duchenne Muscular Dystrophy (DMD) is a rapidly progressive, lethal
neuromuscular disorder, present from birth, which occurs almost exclusively in males. We …