There may be hope for children with a genetic form of muscular dystrophy.
The Child Neurology Center of Northwest Florida is participating in a new research study of an investigational drug for children who have Duchenne/Becker muscular dystrophy.
Duchenne muscular dystrophy is an inherited disorder, characterized by rapidly worsening muscle weakness that starts in the legs and pelvis, and later affects the whole body.
For more information on this story, see the Sept. 25 issue of Navarre Press or subscribe online.