Genetic abnormalities cause a range of muscle diseases called muscular dystrophies. Muscles weaken over time, decreasing mobility and making easy tasks difficult to perform. Muscular Dystrophy (MD) comes in various forms, each affecting a distinct set of muscles, manifests at a different age and has varying degrees of severity.
A person may become the initial family member to develop Muscular Dystrophy, or it may run in families. Each form of Muscular Dystrophy may have several distinct genetic subtypes, and individuals with the same type of Muscular Dystrophy will have a variety of symptoms.
The main indication of this condition is progressive muscle weakness that begins at different ages and in different groups of muscles. Common symptoms of Muscular Dystrophy are:
Muscular Dystrophy is caused by abnormal gene mutations that interfere with the production of proteins needed to form health muscle. For instance, individuals with Duchenne or Becker muscular dystrophies produce insufficient amounts of dystrophin, a protein that strengthens muscles and guards against damage.
Some forms of Muscular Dystrophy are apparent from birth or develop during childhood and some forms arise later during adulthood. Muscular Dystrophy is considered a rare condition with roughly 1 in 6,000 people being diagnosed with MD worldwide.
You or your child might be subjected to one or more of the following diagnostic procedures if your doctor suspects that you or your child has Muscular Dystrophy:
Muscular Dystrophy can affect people of all races, ages, and genders. Yet the most prevalent type, Duchenne, typically affects young males. Progressive muscle weakening has several side effects, including:
With time, disease symptoms of Muscular Dystrophy can worsen, but some therapies can help, such as:
Regrettably, there is no way to stop someone from developing muscular Dystrophy. If you have the condition, taking the following actions can improve your quality of life:
Unfortunately, Muscular Dystrophy is a progressive disease and symptoms tend to worsen over time. There is no cure for this disease, treatment can help improve the quality of life for people living with it.