What is muscular dystrophy?
Muscular dystrophy (MD) is a broad term that describes a genetic (inherited) disorder
of the muscles. Muscular dystrophy causes the muscles in the body to become very weak.
Over time, the muscles break down and are replaced with fatty deposits.
Other health problems commonly associated with muscular dystrophy include:
Breathing and lung problems
Scoliosis— a lateral, or sideways, curvature and rotation of the back bones (vertebrae),
giving the appearance that the person is leaning to one side
Diet, nutrition, and digestive problems
Emotional and mental health issues
The most common forms of muscular dystrophy are Duchenne muscular dystrophy (DMD)
and Becker muscular dystrophy. The two forms are very similar, but Becker muscular
dystrophy is less severe than DMD. Girls are rarely affected by either of these forms
of muscular dystrophy.
What causes muscular dystrophy?
Duchenne muscular dystrophy is a genetic disease which means it is inherited.
There are normally 46 chromosomes in each cell of our body, or 23 pairs. The first
22 pairs are shared in common between males and females, while the last pair determine
gender and are called the sex chromosome pair. Females have two X chromosomes, while
males have one X and one Y chromosome.
Duchenne muscular dystrophy is caused by an X-linked recessive gene. "X-linked" means
that the gene causing the trait or the disorder is located on the X chromosome. Genes
on the X chromosome can be recessive or dominant. X-linked recessive genes are expressed
in females only if there are two copies of the gene (one on each X chromosome). However,
for males there only needs to be one copy of an X-linked recessive gene in order for
the trait or disorder to be expressed. For example, a woman can carry a recessive
gene on one of the X chromosomes unknowingly, and pass it on to a son, who will express
the trait or disease.
What are the symptoms of muscular dystrophy?
Muscular dystrophy is usually diagnosed in children between 3 and 6 years of age.
Early signs of the illness include a delay in walking, trouble rising from a sitting
or lying position, and frequent falling. Weak shoulder and pelvic muscle are also
early symptoms. These are the most common symptoms of muscular dystrophy:
Trouble climbing stairs
Frequently trips and falls
Unable to jump or hop normally
Tip toe walking
Inability to close eyes or whistle
Shoulder and arm weakness
Trouble getting up from a seated position on the floor
A telltale clinical characteristic for Duchenne muscular dystrophy (DMD) is Gowers'
sign. Children with Duchenne muscular dystrophy find it very hard to get up from a
sitting or lying position on the floor. They first pull up to their hands and knees.
The child walks his or her hands up their legs to brace themselves as they rise to
a standing position.
In addition, children with muscular dystrophy often have very large calves due to
the large amounts of fatty deposits that are replacing muscle.
The symptoms of muscular dystrophy may look like other conditions or medical problems.
Always see your child's doctor for a diagnosis.
How is muscular dystrophy diagnosed?
The diagnosis of muscular dystrophy is made with a physical exam and certain tests.
During the exam, your child's doctor takes a complete prenatal and birth history of
the child and asks if other family members are known to have muscular dystrophy.
Tests for muscular dystrophy may include:
Blood tests. These include genetic blood tests.
Muscle biopsy. The primary test used to confirm diagnosis. A small sample of muscle
tissue is taken and examined under a microscope.
Electromyogram (EMG). A test to check if the muscle weakness is a result of destruction
of muscle tissue rather than nerve damage.
Electrocardiogram (ECG). A test that records the electrical activity of the heart,
shows abnormal rhythms (arrhythmias or dysrhythmias), and detects heart muscle damage.
Treatment for muscular dystrophy
Treatment will depend on your child’s symptoms, age, and general health. It will also
depend on how severe the condition is.
To date, there is no known treatment, medicine, or surgery that will cure muscular
dystrophy, or stop the muscles from weakening. The goal of treatment is to prevent
deformity and allow the child to function as independently as possible.
Nonsurgical treatment options include:
Positioning aids used to help the child sit, lie, or stand
Braces and splints used to prevent deformity, promote support, or provide protection
Medications (research trials may help advance treatment)
In some cases, surgery may be considered to manage the following conditions:
Long-term outlook for a child with muscular dystrophy
Muscular dystrophy is a progressive condition that needs life-long management to prevent
deformity and complications. Walking and sitting often becomes more difficult as the
child grows. Usually by the age of 12, the child needs a wheelchair because the leg
muscles are too weak to work. Heart or lung problems often occur by the late teenage
years or into the early 20s.
The interdisciplinary healthcare team will work with your family to improve your child's
functional outcomes and to provide support as you learn to care for your child's needs.
The Muscular Dystrophy Association can be an important resource, both financially
and emotionally, for parents of children with muscular dystrophy.