Becker muscular dystrophy
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Becker muscular dystrophy is an inherited disorder that involves slowly worsening muscle weakness of the legs and pelvis.
Benign pseudohypertrophic muscular dystrophy; Becker's dystrophy
Becker muscular dystrophy is very similar to Duchenne muscular dystrophy, except that it gets worse at a much slower rate and it is less common.
The disorder is passed down through families (inherited). Having a family history of the condition raises your risk.
Becker muscular dystrophy occurs in about 3 to 6 out of every 100,000 births. The disease is found mostly in boys.
Females rarely develop symptoms. Males will develop symptoms if they inherit the defective gene. Symptoms usually appear in boys between ages 5 and 15, but may begin later.
Muscle weakness of the lower body, including the legs and pelvis area, slowly gets worse, causing:
- Difficulty walking that gets worse over time; by age 25-30, the person is usually unable to walk
- Frequent falls
- Difficulty getting up from the floor and climbing stairs
- Difficulty with running, hopping, and jumping
- Loss of muscle mass
- Toe walking
- Muscle weakness in the arms, neck, and other areas is not as severe as in the lower body
Other symptoms may include:
- Breathing problems
- Cognitive problems (these do not get worse over time)
- Loss of balance and coordination
Exams and Tests
The health care provider will do a nervous system (neurological) and muscle examination. A careful medical history is also important, because symptoms are similar to those of Duchenne muscular dystrophy. However, Becker muscular dystrophy gets worse much more slowly.
An exam may find:
- Abnormally developed bones, leading to deformities of the chest and back (scoliosis)
- Abnormal heart muscle function (cardiomyopathy)
- or irregular heartbeat () - rare
- Muscle deformities, including contractures of heels and legs, abnormal fat and connective tissue in calf muscles
- Muscle loss that begins in the legs and pelvis, then moves to the muscles of the shoulders, neck, arms, and respiratory system
Tests that may be done include:
There is no known cure for Becker muscular dystrophy. The goal of treatment is to control symptoms to maximize the person's quality of life. Some doctors prescribe steroids to help keep a patient walking for as long as possible.
Activity is encouraged. Inactivity (such as bed rest) can make the muscle disease worse. Physical therapy may be helpful to maintain muscle strength. Orthopedic appliances such as braces and wheelchairs may improve movement and self-care.
Genetic counseling may be recommended. Daughters of a man with Becker muscular dystrophy may carry the defective gene and could pass it on to their sons.
Becker muscular dystrophy leads to slowly worsening disability, although the amount of disability varies. Some men may need a wheelchair, while others may only need to use walking aids such as canes or braces.
Lifespan is usually shortened if there is heart and breathing disease.
- Heart-related problems such as cardiomyopathy
- Lung failure
- or other infections
- Increasing and permanent disability that leads to decreased ability to care for self, decreased mobility
When to Contact a Medical Professional
Call your health care provider if:
Genetic counseling may be advised if there is a family history of Becker muscular dystrophy.
Kliegman RM, Behrman RE, Jenson HB, Stanton BF. Muscular dystrophies. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 608.
- Last reviewed on 2/24/2014
- Joseph V. Campellone, M.D., Division of Neurology, Cooper University Hospital, Camden, NJ. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editrial team.
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