Muscular dystrophy is a genetic disorder that reason progressive muscle paleness and loss of muscle mass, mainly in the skeletal muscles, such as persons in the arms and legs. But muscular dystrophy can also disturb muscles in the face, in the heart, the muscles that control breathing, and, actually, any muscle in the body.
In some cases, the illness also disturbs brain function. Signs of the most common variations of muscular dystrophy start in childhood, although less-common diversities may not cause indications until adulthood. Stem cell treatment for muscular dystrophy is one of the best treatment options for treating this particular illness. Below, I’m going to share some complications of muscular dystrophy.
Common Complications of Muscular Dystrophy
- Contractures
Contractures are the shortening of muscles or tendons around the joints, and they can further limit flexibility. Regular widening and range-of-motion movements can delay contractures, but if they become simple, your doctor may commend surgery, which may reestablish some joint role and decrease discomfort.
- Breathing Difficulties
As its development, muscular dystrophy may disturb the muscles related to breathing. As a result, a person with muscular dystrophy may need to use a living device (a ventilator), possibly primarily only at night but probably also during the day.
- Swallowing Difficulties
Progressive muscle paleness may harmfully affect the capability to swallow when eating or drinking. Some of the possible significances of swallowing problems contain nutrient lack and a disorder called aspiration pneumonia, in which food can get stuck in the lungs, leading to pneumonia, and lung contamination.
These are some common complications of muscular dystrophy. You can find one of the most recognised hospitals to take stem cell treatment for muscular dystrophy.