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 …

Background Duchenne muscular dystrophy (DMD) is a severe rare progressive inherited
neuromuscular disorder, leading to loss of ambulation (LOA) and premature mortality. The …

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Duchenne muscular dystrophy (DMD) is the most common paediatric muscle condition.
Affected boys show first symptoms around the age of 2–5 years with progressive muscle …

Background Duchenne muscular dystrophy (DMD) is a rare, severe, fatal neuromuscular
disease characterized by progressive atrophy and muscle weakness, resulting in loss of …

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 inherited neuromuscular disorder of
childhood and mainly affects males. Over the course of the last century, the average life …

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 …