Impact of COVID-19 on Duchenne Muscular Dystrophy (DMD) Treatment Market to Witness Robust Expansion
Duchenne Muscular Dystrophy (DMD) is a rare hereditary disease that affects the muscles and the connective tissue of the body. This condition is usually identified through skin tests and in more severe cases, it can be detected through MRI. The symptoms include drooping eyelids, decreased muscle bulk, weak pulse, and slow heart rate. The cause of this disease is not yet known but it is believed to be due to genetic differences, abnormalities in the nervous system, and infection.
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