One specific type of CMD is LAMA2-related muscular dystrophy (LAMA2-MD), which is caused by mutations in the LAMA2 gene. This condition not only affects muscle function but can also lead to ...

The gene therapy delandistrogene moxeparvovec-rokl showed clinically meaningful benefits and disease stabilization at 2 years ...

The data showed reduced difficulties in standing, walking and running that were statistically significant, the company said.

The FDA has granted fast-track designation to an investigational antisense oligonucleotide to treat individuals with myotonic ...

Muscular dystrophy (MD) represents a group of inherited muscle disorders that primarily cause muscle weakness and muscle wasting, though some types of the disease also present with other ...

Muscle strength grading is used to categorize muscle strength on a scale of 0 to 5 in relation to the expected strength for a muscle. One of the more common methods is a hands-on test called the ...