Duchenne Muscular Dystrophy in Children
What is Duchenne muscular dystrophy in children?
Duchenne [doo-SHEN] muscular dystrophy (DMD) is a rare genetic condition that weakens
your child’s muscles. It is the most common muscular dystrophy, a kind of inherited
muscle disease. DMD causes weakness and muscle loss that spreads throughout your child’s
DMD appears in young boys, usually
between ages 2 and 5. It causes muscle loss that gets worse over time. Most boys with
DMD need a wheelchair by the time they are teenagers. DMD damages the muscles needed for
movement. DMD also can weaken the heart muscle and make the heart enlarge (dilated
cardiomyopathy). DMD has no cure, but some people with DMD can live into their 40s and
What causes Duchenne muscular dystrophy in a child?
DMD is caused by changes (mutations) in the gene that helps make dystrophin. Dystrophin
is an important protein in muscle cells. It helps keep the muscle fibers stable and
Muscles are made up of bundles of long muscle fibers (muscle cells). These fibers pull
together (contract) when nerve signals from the brain travel to the specific spot
(junction) where the nerve activates the muscle. Dystrophin is part of a complex set of
proteins that normally protect your child’s muscle fibers as they contract and
In DMD, the gene changes cause your
child's body to make very little or no dystrophin. Without enough dystrophin, the
muscle cells become leaky and die. This causes the muscles to weaken. If the gene can
still make some dystrophin, the condition has milder symptoms. This is called Becker
muscular dystrophy. People with DMD generally don’t have any dystrophin at all.
DMD generally affects boys because the dystrophin gene is on the X
chromosome. Chromosomes are the parts of your cells that contain your
genes. Boys only have one X chromosome. Girls have two X chromosomes, one from each
parent. Boys get one X chromosome from their mother and one Y chromosome from their
father. The condition only rarely affects girls.
Because a boy only has one copy of
the dystrophin gene, a DMD mutation means that he will not have enough dystrophin to
keep his muscles working well. For this reason, DMD is called an X-linked condition.
When a girl inherits a DMD mutation on one of her X chromosomes, she usually gets enough
dystrophin from a healthy gene on the other X chromosome. But some girls don’t have
quite enough dystrophin. This causes mild to moderate DMD symptoms and disease of the
heart muscle (cardiomyopathy).
Women who have a DMD mutation are DMD carriers. They have a 1 in 2 chance of passing
the gene on to each child. If a boy gets the mutation, he gets the disease. A girl who
gets the mutation will be a carrier. A mutation can also sometimes happen without being
passed on from a parent. This is called a de novo mutation.
What are the symptoms of Duchenne muscular dystrophy in a
Muscle weakness begins in young children. It affects the hips and thighs before
spreading to the arms and the rest of the body. First signs and symptoms of DMD in
preschoolers may include:
- Trouble with running, jumping, and climbing stairs
- Using hands to get up from sitting or squatting. This is a movement called Gower’s
- Enlarged calves
- Leg pain
- Learning problems
As the disease gets worse, DMD can lead to:
- Broken bones from falling
- Greater need for a wheelchair
- Curving of the spine (scoliosis)
- Stiff joints that can’t move (contractures)
- Tiredness (fatigue) and weakness
- Shortness of breath or other breathing problems
- Irregular heartbeat or other heart problems
How is Duchenne muscular dystrophy diagnosed in a child?
Your child’s healthcare provider
will take a full health history, and ask about current symptoms and past health
conditions. He or she will ask about related conditions in the family. He or she usually
does a physical exam and lab tests. Your child may need tests that include:
- Blood tests, for muscle enzymes such as creatine kinase
- DNA blood tests, for dystrophin changes
- Dystrophin analysis, a blood test that looks at your dystrophin
- Electromyography, to measure the electrical activity of the muscles
- MRI or ultrasound, to look at the muscles
- Muscle biopsy, to look at the muscle cells or confirm a diagnosis
Your child may first see his or her
main healthcare provider and then be diagnosed by a neurologist. Some neurologists have
special training to treat nerve and muscle diseases such as DMD. Your child may also
need care from other providers such as cardiologists, pulmonologists, and physical
How is Duchenne muscular dystrophy in a child treated?
DMD has no cure, but many supportive treatments can help manage the condition. Some
possible treatments for children with DMD include:
- Steroid medicine. This may help slow loss of muscle.
- Heart medicines. These can help treat cardiomyopathy.
- Pacemakers or other heart devices. These can help keep the heartbeat regular.
- Breathing devices. These can help your
child get enough air. Many people with DMD sleep with a breathing machine mask at
night. Your child may also need a tracheostomy device.
- Range-of-motion exercises. These can
help your child stay flexible and limit contractures of the joints. Gentle exercise
like water exercises may be safe. Your child’s healthcare team can help design a safe
exercise program for your child.
- Surgery can ease contractures or straighten a curved spine. But children with DMD
have extra risks with anesthesia.
Advances in care have improved the life expectancy for people with DMD. Researchers are
working on developing new medicines.
What are possible complications of Duchenne muscular dystrophy
in a child?
In addition to muscle weakness throughout the body, DMD can cause serious problems for
the heart and lungs. Your child may need these tests:
- Breathing tests
- Echocardiograms to see how well your child’s heart is working
- Electrocardiograms to check heart rhythms
- Swallowing studies to check for problems that affect eating
- X-rays to look for scoliosis
- Bone scans to watch bone health
Can Duchenne muscular dystrophy in a child be prevented?
Because DMD is a genetic disorder, you can’t do much to prevent it. But if DMD runs in
your family, you may consider talking with a genetic counselor and getting testing
before having children. If you or your partner has the DMD change, you may decide to
check your fertilized eggs and only implant those that do not have DMD. If you or your
partner recently got pregnant, you can also choose to test the fluid outside the fetus
to see if the fetus has DMD.
How can I help my child live with Duchenne muscular
Work with your child’s healthcare
provider and his or her healthcare team. Your child may need healthcare providers that
can help with the neuromuscular, orthopedic, respiratory, and heart problems of DMD.
Your family may get help from social and mental health support.
Physical therapists and occupational therapists can help your child keep his or her
independence and mobility as the condition gets worse.
While your child can still walk, some helpful therapies include:
- Range-of-motion movements of the ankle, hip, and knee joints to keep mobility
- Lower-leg braces and hand splints to prevent contractures
- Lightweight manual wheelchair for long distances
Once your child is using a wheelchair full-time, the following may also help:
- Range-of-motion movements of the shoulder, elbow, wrist, and finger joints, in
addition to the leg joints
- Powered wheelchair
- Mechanical lift
- Special powered beds
You and your family may want to look for more information on your child’s condition
at the Muscular Dystrophy Association.
Key points about Duchenne muscular dystrophy in children
- DMD is a genetic disease of young boys that causes muscle weakness throughout the
- DMD is caused by a defect in the gene that helps make dystrophin. This is a protein
that plays a key role in protecting muscle fibers.
- Symptoms include muscle weakness. You may notice that your child has trouble
running, jumping, or climbing stairs.
- A healthcare team can help your child manage the different aspects of DMD.
Tips to help you get the most from a visit to your child’s healthcare provider:
- Know the reason for the visit and what you want to happen.
- Before your visit, write down questions you want answered.
- At the visit, write down the name of a new diagnosis, and any new medicines,
treatments, or tests. Also write down any new instructions your provider gives you for
- Know why a new medicine or treatment is prescribed and how it will help your child.
Also know what the side effects are.
- Ask if your child’s condition can be treated in other ways.
- Know why a test or procedure is recommended and what the results could mean.
- Know what to expect if your child does not take the medicine or have the test or
- If your child has a follow-up appointment, write down the date, time, and purpose
for that visit.
- Know how you can contact your child’s provider after office hours. This is important
if your child becomes ill and you have questions or need advice.
Online Medical Reviewer:
Anne Fetterman RN BSN
Online Medical Reviewer:
Joseph Campellone MD
Online Medical Reviewer:
Raymond Kent Turley BSN MSN RN
Date Last Reviewed:
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