January 31, 2020. Steroid therapy is a standard treatment for Duchenne, while other treatments will depend on your specific symptoms and condition. Some forms of MD involve the heart. They control its symptoms and even slow them down. Right now, there are two approved steroids for Duchenne: prednisone and Emflaza (deflazacort). We comply with the HONcode standard for trustworthy health information -. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. They persist throughout life. The disorders differ in which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. A pacemaker can help to maintain a normal heart rate. Myotonic dystrophy is the most common adult form of muscular dystrophy. Gene therapy is just one strand of research into treating muscular dystrophy. In a person who hasn't had a traumatic injury, high blood levels of CK suggest a muscle disease — such as muscular dystrophy. June 13, 2020. What Are the Best Treatment Options for Duchenne Muscular Dystrophy? While these drugs have been shown to extend muscle function, including the ability to walk, they have many unpleasant side effects. Treating Duchenne means tackling all the problems that can arise from the condition, from muscle tightness to cardiovascular and breathing problems. It places additional strain on their weak muscles. Patients are given supportive care, leg braces and physiotherapy to help them function in daily life. Myostatin inhibitors are one such possible therapy. Unfortunately, there is no known cure for muscular dystrophy (MD), but researchers are making advances that continue to improve the quality of lives of people living with the disease. However, some people cannot tolerate this medication. It’s important to monitor the progression of scoliosis both visually and by X-ray, says Rao. There’s no known cure for muscular dystrophy, but certain treatments may help. Several potential therapies aim to promote muscle growth to combat the deterioration seen in MD patients. “Usually, when I can convince parents to start younger, it’s when they’ve already had a boy with Duchenne who stopped walking a lot younger than is typical, like age 7,” she notes, referring to older brothers who also have Duchenne. Physical therapy, stretching, and range-of-motion exercises Working with a physical therapist, and doing recommended stretches and exercises at home, is key to maintaining as much strength and flexibility as possible, says Rao — regardless of your disease progression or mobility status. Mayo Clinic. Based on the form of muscular dystrophy you get, different muscular dystrophy treatments will be recommended by your doctor. A rare condition and a group of congenital diseases that causes mutilation and muscle weakness is called muscle dystrophy. An estimated 975,000 to 3 million people worldwide have been diagnosed with the most common type of muscular dystrophy, myotonic dystrophy … Ideally, a multidisciplinary healthcare team will take many different approaches to ensure that all of your needs and concerns are addressed. Others have severe symptoms and die at a young age. Your doctor will review your (or your child's) medical history and symptoms. Duchenne muscular dystrophy is a genetic, progressive condition that causes loss of muscle function over time. Steroid medication for Duchenne MD is available in tablet or liquid form, and current research suggests a daily dose is most effective. However, most of the people with muscular dystrophy do lose the ability to walk and eventually require a wheelchair. The disease affects the muscles with definite fiber degeneration but without evidence of morphologic aberrations. Muscular dystrophy (MD) refers to a group of genetic diseases described by progressive dysfunction and/or weakness of skeletal muscles. Damaged muscles release enzymes, such as creatine kinase (CK), into your blood. Everyday Health is among the federally registered trademarks of Everyday Health, Inc. and may not be used by third parties without explicit permission. http://www.mdausa.org/, Parent Project for Muscular Dystrophy Research People whose LGMD has reached this stage often find that a great deal of their independence returns and fatigue is greatly reduced when they begin using this type of mobility equipment. When chest muscles are involved in MD, respiratory therapy may be used to delay breathing problems. Unlike the other muscular dystrophies, the muscle weakness is accompanied by myotonia (delayed relaxation of muscles after contraction) and by various other non-muscular symptoms. There are many research studies investigating medical treatments for limb girdle muscular dystrophy. Muscular dystrophy is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time. Available for Android and iOS devices. The doctor will do a neurological examination to look for nerve problems. Over time, Duchenne tends to weaken the muscles that control breathing. It’s considered standard to start it by age 4 or 5, says Ramos-Platt, but starting at age 2 or 3 is more controversial. Causes: Duchenne muscular dystrophy affects most commonly in children especially males. Duchenne muscular dystrophy is an inherited disorder that involves muscle weakness, which quickly gets worse. It effects people of all the age group. 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