New study shines light on DMD symptoms in women
A new study suggests that some female carriers of Duchenne muscular dystrophy (DMD) mutations experience symptoms and complications.
A new study suggests that some female carriers of Duchenne muscular dystrophy (DMD) mutations experience symptoms and complications.
A 16-year-old boy with Duchenne muscular dystrophy (DMD) died of acute liver failure several months after receiving Elevidys, a gene therapy.
A recent systematic review highlighted the risks associated with various anesthetic techniques in patients with DMD.
Parents of patients with DMD exhibit some positive psychological and emotional growth, but would benefit from better support systems.
Young adults with DMD want to live meaningful, independent adult lives, but face challenges in social participation.
Researchers identified two previously unreported mutations in the Dystrophin gene, providing new insights into muscular dystrophy.
Patients with Duchenne muscular dystrophy (DMD) who can walk beyond the age of 12 appear to have better cardiac function during adulthood.
Patients of different racial and ethnic backgrounds with DMD received different treatments and had varying health care costs.
A recent study used administrative health records to follow patients with DMD long-term and assess key clinical outcomes.
Researchers found that children with DMD may have reduced social cognition, an understudied element of neuropsychological function.