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) 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 the most common severe heritable muscle disorder
of childhood. Affected boys show first symptoms around the age of 2–5 years with …

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

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 (DMD) is an X-linked disorder for which there is currently no
curative treatment. The natural history is such that affected boys need to use a wheelchair at …

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 an X-linked genetic disorder that causes
progressive weakness and wasting of skeletal muscular and myocardium in boys due to …

Aim: Duchenne muscular dystrophy (DMD) is a severe and rare X-linked neuromuscular
childhood disorder that results in functional decline, loss of ambulation and early death due …