The symptoms of Becker muscular dystrophy (BMD) may begin anywhere from childhood to a person's early 20s. "How is muscular dystrophy diagnosed?" Duchenne muscular dystrophy (DMD) is the most common type. https://www.uptodate.com/contents/search. https://www.ninds.nih.gov/Disorders/All-Disorders/Muscular-Dystrophy-Information-Page. Other types don't surface until adulthood. ", FDA News Release. The absence of this protein is linked with so many problems. You may want to ask: Right now, there’s no cure for the disease. They can help your child connect with others like them and give you and your family advice and understanding. Emery-Dreiffuss muscular dystrophy: It mostly affects children. Neurological disorders and cardiovascular disease. Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. 1. MD can begin in infancy or childhood, or later in life. In its most … Most people’s condition will get worse over time, and some people may lose the ability to walk, talk, or care for themselves. You’ll want to find out as much about your child’s condition as you can to learn how they can stay as healthy as possible. The most of this condition is Duchenne. Make a donation. Muscular dystrophy causes the gradual weakening of skeletal muscle. Signs and Symptoms What happens to someone with distal muscular dystrophy (DD)? Leg muscles become increasingly weaker. These tests confirm the diagnosis and determine the type of muscular dystrophy: Creatine kinase (CK) level: This blood test checks the level of creatine kinase, a protein that normally stays inside muscle cells. Muscular Dystrophy Symptoms and Treatment Muscular dystrophy is a group of genetic conditions in which muscles become weak and wasted. The child also has trouble walking or running normally. They often are a way for people to try new medicine that isn't available to everyone. A protein known as dystrophin is essential for the normal functioning of muscles, the deficiency of this protein weakens the muscles and their working. Some types affect mostly boys while other types affect both boys and girls. Do they have a hard time walking or doing their usual activities? Muscular dystrophy occurs in both sexes and in all ages and races. You can get muscular dystrophy even if neither of your parents had the disease. Muscular dystrophy is a challenge, but it doesn’t have to keep your child from enjoying life. With time, other muscle groups may become affected as well. The disease will most likely have a big impact on your family. Duchenne and Becker muscular dystrophy: Clinical features and diagnosis. However, it's often the smaller muscles that are affected first, such as those in the face, jaw and neck. Many people will eventually become unable to walk. This site complies with the HONcode standard for trustworthy health information: verify here. Support groups are also good places to talk to other people who have lived with muscular dystrophy. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle. Any use of this site constitutes your agreement to the Terms and Conditions and Privacy Policy linked below. They may ask: They also may ask you questions about how your child plays, moves, and speaks, as well as how they act at home and at school. Talk to your doctor about your child’s muscular dystrophy. There's no cure for muscular dystrophy. "FDA grants accelerated approval to first drug for Duchenne muscular dystrophy. Although girls can be carriers and mildly affected, it's much more common in boys. Spasticity management for spinal cord injury, Muscular dystrophy, Spinal cord injury, Gait unsteadiness, Spasticity, Pe... diatric trauma, Spina bifida, Cerebral palsy, Acquired brain disorder, Traumatic brain injury. 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