Cellular therapy in dmd

Duchenne muscular dystrophy (DMD) is a rare muscle disorder however it is one of the most common genetic conditions affecting about 1 in 3,500 male worldwide...

Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder. It occurs due to mutations in the dystrophin gene. It is characterized by progressive muscle weakness and wasting due to the absence of dystrophin protein in the muscles that causes degeneration of skeletal and cardiac muscles.

Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder. It occurs due to mutations in the dystrophin gene. It is characterized by progressive muscle weakness and wasting due to the absence of dystrophin protein in the muscles that causes degeneration of skeletal and cardiac muscles. Genetic analysis of DMD patients show deletions/duplications in the exons of dystrophin gene.

Cellular therapy in dmd, Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy that primarily affects boys. Muscle weakness usually begins around the age of four, and worsens quickly. Muscle loss typically occurs first in the thighs and pelvis followed by the arms. Dr Rajput...

Duchenne muscular dystrophy (DMD) is an X-linked inherited neuromuscular disorder. It occurs due to mutations in the dystrophin gene. It is characterized by ...

DMD is a genetic disorder which causes muscle power loss in boys. It's final treatment would definitely be Genetic engineering or gene therapy but it would be helpful to undamaged muscle only. so currently doctors need to protect muscles by some regenerative method like Autologous bone marrow cell transplant.

Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). These forms of muscular dystrophy occur almost exclusively in males. Duchenne Muscular Dystrophy (DMD) is an X-linked recessive...