Center for Genetic Muscle Disorders: Patient Care Approach
As a first step, we discuss the onset and progression of symptoms, examine muscles and other organ systems, and review any previous testing. Our team may recommend a blood test or muscle biopsy. A genetic counselor guides patients through the diagnostic process. Once a diagnosis has been confirmed, we tailor a treatment plan to the needs of each patient. The team may provide medical management through the use of corticosteroids or other drugs, which need to be carefully monitored. In addition, patients receive an assessment and individualized rehabilitation treatment plan. The team also manages contractures (shortening of the muscle or tendon), scoliosis, and heart and lung function. Finally, to help ensure each patient’s success in community life, our social worker assists patients and families in securing any needed social, financial, and educational support.
To learn more about the Center and how it’s serving patients:
- Listen to Dr. Wagner’s podcast introducing the Center for Genetic Muscle Disorders
- Read our Potential Magazine article - "A Family’s Journey: Kennedy Krieger’s new Center for Genetic Muscle Disorders helps mother and son live with muscular dystrophy"
Center Families & Staff Run to End Duchenne
JUNE 18, 2016
Center News & Updates
"In My Mind" Artwork Exhibit
A collection of artwork by individuals with Duchenne muscular dystrophy representing a wide array of interests, techniques, styles, and perspectives.
News & Updates
A free resource that provides access to information and support for individuals and families living with developmental disabilities.