Types of Treatments for Muscular Dystrophy
Muscular dystrophy encompasses a set of disorders that lead to a progressive loss in muscle mass, resulting in the loss of strength. The most common variety of muscular dystrophy is Duchenne muscular dystrophy, which primarily strikes young boys. Genetic mutations are one of the primary causes of this medical condition. These mutations interfere with the creation of proteins in the muscles, without which muscles cannot be built or remain healthy. Causes for muscular dystrophy are typically genetic, and unfortunately, treatments for muscular dystrophy are not 100% effective. Treatments can only alleviate the symptoms, but cannot cure the condition. The doctor will test the blood for enzymes that get released by the affected muscles and for genetic markers. An electromyography test uses an electrode needle for detecting muscle electrical activity. A muscle biopsy may also be conducted for diagnosis, where a sample of the muscle is tested. 1. Surgery The general treatments for muscular dystrophy include surgeries to correct muscle shortening and assisted ventilation when the respiratory muscles get damaged. Surgery may also be required for correcting spinal curvatures that often cause difficulty in breathing. 2. Medications There are medications for heart ailments, surgery for repairing cataracts, and treating scoliosis. Doctors may recommend eteplirsen, which is the first FDA-approved medicine for treating Duchenne muscular dystrophy.