Dystrophy is any condition in which a part of the body weakens or wastes away. In muscular dystrophy, the weakness is in the muscles. An inherited genetic mistake prevents the body from making a protein that helps build muscles and keep them strong.
Children who are born with muscular dystrophy usually develop normally for the first few years of life. They may suddenly show signs of clumsiness. These signs include:
Sometimes children’s allergy symptoms don’t stop with a stuffy nose and watery eyes. If your child has allergic asthma, the most common form of asthma, exposure to allergens like pollen and mold can cause breathing passages to become swollen and inflamed. Childhood allergies that trigger asthma can lead to wheezing, shortness of breath, and difficulty breathing.
When that happens, your child’s doctor may prescribe the use of a breathing machine called a nebulizer. The following Q & A will help...
difficulty raising the front of their foot (called foot drop)
Over time, children with muscular dystrophy can become weaker and weaker, losing the ability to sit, walk, and lift objects. Because the disease can also affect muscles in the heart and lungs, serious heart and breathing problems can occur.
There are several different types of muscular dystrophy. Muscle weakness is a hallmark of each type. But the symptoms can vary and start at different ages.
Some muscular dystrophies are mild. Others are severe and cause greater muscle loss.