Muscular dystrophy (MD) is a group of inherited diseases that cause muscle weakening and a loss of muscle tissue. The body replaces the lost muscle tissue with fat and connective tissue. The muscle weakness makes it hard or even impossible for your child to walk.
There are many forms of muscular dystrophy. Duchenne muscular dystrophy (DMD) is the most common type. It is also the most severe childhood form of the disease.
MD can affect the heart. Also, as the breathing muscles weaken, a child may start having lung problems, including pneumonia.
Currently, there is no cure for this disease. The life span for people with MD is usually shorter than normal.
What is the cause?
MD is a genetic disorder. This means that it is caused by a problem with one or more genes. Genes are inside each cell of your body. They contain the information that tells your body how to develop and work. Changes in the genes can be passed from parents to children.
Children who have MD have a problem with a gene that makes a protein needed by their muscles. Without this protein, or the right form of the protein, their muscles donâ€™t work right.
One or both parents may be a carrier of the defective gene and pass it on to their child. A carrier is a person who has the faulty gene but usually shows no symptoms of the disease.
Because of the way DMD is inherited, it affects mostly boys. Symptoms are rare in girls. However, girls can be carriers.
What are the symptoms?
Symptoms start in early childhood, usually between the ages of 3 and 5 years. Symptoms may include:
Clumsiness and frequent falls
Trouble getting up from the floor or getting up after lying down
An unusual, waddling gait when your child walks
Problems with learning
Changes in muscle size
How is it diagnosed?
Your childâ€™s healthcare provider will ask about your childâ€™s symptoms and medical history and examine your child. Tests may include:
Muscle biopsy, which is the removal of a small sample of tissue for testing
Tests of the muscle and nerves
How is it treated?
Treatment is focused on managing the symptoms of muscular dystrophy with:
Exercise programs and physical therapy so there is less muscle shortening around the joints
Leg braces and use of wheelchairs and walkers
Surgery to relieve muscle shortening and curving of the spine
Medicine may include:
Steroids to slow the breakdown and loss of muscles tissue
Medicines called immunosuppressants to slow damage to muscle cells
If it gets hard for your child to breathe, your child may use a machine that helps breathing, especially at night.
Many experimental therapies have not yet shown proven benefits. However, researchers are working hard to find better treatments and a cure for this disease.
How can I take care of my child?
You may need to make some changes in your childâ€™s diet.
Your childâ€™s diet should be high in fluid and fiber, with lots of fresh fruits and vegetables to prevent constipation (bowel movements fewer than 3 times a week).
If your child is taking a steroid or has heart problems, he may need to cut back on sodium (salt) in the diet.
Children who use power wheelchairs, take a steroid, or are not very active should have a low-calorie diet to keep their weight down. Being overweight can stress weakened muscles and the heart. A low-calorie diet does not hurt the muscles.
Follow your childâ€™s healthcare provider’s instructions. Ask your provider:
How and when you will hear your childâ€™s test results
What activities your child should avoid and when your child can return to normal activities
How to take care of your child at home
What symptoms or problems you should watch for and what to do if your child has them
Make sure you know when your child should come back for a checkup.
Written by Robert Brayden, MD, Professor of Pediatrics, University of Colorado.
Pediatric Advisor 2015.1 published by RelayHealth. Last modified: 2013-05-14 Last reviewed: 2013-02-07
This content is reviewed periodically and is subject to change as new health information becomes available. The information is intended to inform and educate and is not a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional.