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

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

Muscular dystrophies are a clinically and heterogeneous group of disorders that all share
clinical characteristics of progressive muscular weakness. Duchenne muscular dystrophy …

Background Duchenne muscular dystrophy (DMD) is the most common hereditary muscular
dystrophy and caused by DMD gene mutation. In addition to progressive proximal muscle …

Background: Duchenne muscular dystrophy (DMD) is the most common form of muscular
dystrophy in childhood. Method: To assess the current care of paediatric DMD patients in …

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 among the most common lethal genetic diseases. It
has been proposed that genetic counseling and prenatal diagnosis have begun to lower the …

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 …