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:
When Eleilia Preston gave birth to her first child, the last thing she
worried about was lead in toys.
The stay-at-home mom, who describes herself as "over-the-edge
careful," made sure that little Megan was always within eyesight. She
documented each bite her daughter ate and washed all her toys, several times a
That's why Preston, 29, was so shocked when doctors diagnosed the toddler
with lead poisoning.
At 21 months, Megan far exceeded every developmental milestone for her age
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.
Duchenne Muscular Dystrophy
Duchenne muscular dystrophy is the most common and severe form of the disease. It usually starts when a child is between ages 2 and 5.
Symptoms of Duchenne muscular dystrophy include:
Muscle weakness that begins in the hips, pelvis, and legs
Trouble learning to sit independently and walk
Unsteady, waddling gait
Walking on the toes or balls of the feet
Clumsiness, falling often
Trouble climbing stairs
Difficulty rising from a lying or sitting position
Larger-than-normal calves that are sometimes painful
Learning disabilities or behavioral problems
Curvature of the spine (scoliosis). This can cause one hip to rise higher than the other.
Breathing problems that may eventually require the use of a ventilator
By age 12, most children with Duchenne muscular dystrophy must use a wheelchair to get around. The disease also damages the heart and the muscles needed to breathe, which can be life threatening.
Becker Muscular Dystrophy
The symptoms of Becker muscular dystrophy are similar to those of Duchenne muscular dystrophy. But Becker muscular dystrophy starts later -- around the teen years. It also develops much more slowly.
The first signs of Becker muscular dystrophy may be trouble walking fast, running, and climbing stairs. Other symptoms may include:
Muscle weakness that starts in the pelvis, shoulders, hips, and thighs
Difficulty learning how to walk
Walking on the toes
Muscle cramps when exercising
Trouble lifting objects above waist height because of shoulder and arm weakness
Heart and breathing problems (later in life)
Often children with Becker muscular dystrophy can walk. As they get older they may need to use a cane or wheelchair to get around.
The symptoms of myotonic dystrophy may be obvious from birth or they can develop later -- during the teenage or adult years.