Guide To The Conditions Prednisone Treats

Duchenne Muscular Dystrophy

Duchenne muscular dystrophy is a genetic condition that causes progressive muscle weakness. This form of muscular dystrophy is more common in males, and symptoms tend to begin before the age of six. The muscle weakness associated with this condition often starts in the pelvis and legs, and it tends to be less severe in the arms and neck. Patients could have trouble climbing stairs or getting up from a reclined position, and they might fall frequently. They could also have breathing difficulties and trouble with walking. Many patients with Duchenne muscular dystrophy lose the ability to walk by the age of twelve, and breathing and heart issues typically begin by twenty years old. Genetic tests, muscle biopsies, serum CPK test, and electromyography tests may be used in the diagnostic process. Although there is no cure for muscular dystrophy, treatments can help manage symptoms and improve quality of life. Steroids such as prednisone are administered to reduce the rate of decline in muscle strength, and physical therapy and speech therapy can be helpful as well. Some patients may need breathing assistance at night, and braces and wheelchairs are useful in improving mobility.

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