Home
Duchenne muscular dystrophy is an inherited disorder that involves rapidly worsening muscle weakness.
Causes, incidence, and risk factors
Duchenne muscular dystrophy is a rapidly-worsening form of muscular dystrophy. Other muscular dystrophies (including Becker's muscular dystrophy) get worse much more slowly.
Duchenne muscular dystrophy is caused by a defective gene for dystrophin (a protein in the muscles). However, it often occurs in people without a known family history of the condition.
Because of the way the disease is inherited, males are more likely to develop symptoms than are women. The sons of females who are carriers of the disease (women with a defective gene but no symptoms themselves) each have a 50% chance of having the disease. The daughters each have a 50% chance of being carriers.
Duchenne muscular dystrophy occurs in approximately 1 out of every 3,600 male infants. Because this is an inherited disorder, risks include a family history of Duchenne muscular dystrophy.
Symptoms
Symptoms usually appear before age 6 and may appear as early as infancy. They may include:
Fatigue
Mental retardation (possible, but does not worsen over time)
Muscle weakness
Begins in the legs and pelvis, but also occurs less severely in the arms, neck, and other areas of the body
Difficulty with motor skills (running, hopping, jumping)
Frequent falls
Rapidly worsening weakness
Progressive difficulty walking
Ability to walk may be lost by age 12
By age 10, the person may need braces for walking. By age 12, most patients are confined to a wheelchair.
Signs and tests
A complete nervous system (neurological), heart, lung, and muscle exam may show:
Abnormal heart muscle (cardiomyopathy)
Congestive heart failure or irregular heart rhythm (arrhythmias) -- rare
Deformities of the chest and back (scoliosis)
Enlarged calf muscles, which are eventually replaced by fat and connective tissue (pseudohypertrophy)
Loss of muscle mass (wasting)
Muscle contractures in the heels, legs
Muscle deformities
Respiratory disorders, including pneumonia and aspiration of food or fluid into the lungs (in late stages of the disease)
Tests may include:
Electromyography (EMG)
Genetic tests
Muscle biopsy
Serum CPK
Treatment
There is no known cure for Duchenne muscular dystrophy. Treatment aims to control symptoms to maximize quality of life. Gene therapy may become available in the future.
Activity is encouraged. Inactivity (such as bedrest) can worsen the muscle disease. Physical therapy may be helpful to maintain muscle strength and function. Orthopedic appliances (such as braces and wheelchairs) may improve mobility and the ability to care for yourself.
Expectations (prognosis)
Duchenne muscular dystrophy leads to quickly worsening disability. Death usually occurs by age 25, typically from lung disorders.
Complications
Cardiomyopathy
Congestive heart failure (rare)
Deformities
Heart arrhythmias (rare)
Mental impairment (varies, usually minimal)
Permanent, progressive disability
Decreased mobility
Decreased ability to care for self
Pneumonia or other respiratory infections
Respiratory failure
Causes, incidence, and risk factors
Duchenne muscular dystrophy is a rapidly-worsening form of muscular dystrophy. Other muscular dystrophies (including Becker's muscular dystrophy) get worse much more slowly.
Duchenne muscular dystrophy is caused by a defective gene for dystrophin (a protein in the muscles). However, it often occurs in people without a known family history of the condition.
Because of the way the disease is inherited, males are more likely to develop symptoms than are women. The sons of females who are carriers of the disease (women with a defective gene but no symptoms themselves) each have a 50% chance of having the disease. The daughters each have a 50% chance of being carriers.
Duchenne muscular dystrophy occurs in approximately 1 out of every 3,600 male infants. Because this is an inherited disorder, risks include a family history of Duchenne muscular dystrophy.
Symptoms
Symptoms usually appear before age 6 and may appear as early as infancy. They may include:
Fatigue
Mental retardation (possible, but does not worsen over time)
Muscle weakness
Begins in the legs and pelvis, but also occurs less severely in the arms, neck, and other areas of the body
Difficulty with motor skills (running, hopping, jumping)
Frequent falls
Rapidly worsening weakness
Progressive difficulty walking
Ability to walk may be lost by age 12
By age 10, the person may need braces for walking. By age 12, most patients are confined to a wheelchair.
Signs and tests
A complete nervous system (neurological), heart, lung, and muscle exam may show:
Abnormal heart muscle (cardiomyopathy)
Congestive heart failure or irregular heart rhythm (arrhythmias) -- rare
Deformities of the chest and back (scoliosis)
Enlarged calf muscles, which are eventually replaced by fat and connective tissue (pseudohypertrophy)
Loss of muscle mass (wasting)
Muscle contractures in the heels, legs
Muscle deformities
Respiratory disorders, including pneumonia and aspiration of food or fluid into the lungs (in late stages of the disease)
Tests may include:
Electromyography (EMG)
Genetic tests
Muscle biopsy
Serum CPK
Treatment
There is no known cure for Duchenne muscular dystrophy. Treatment aims to control symptoms to maximize quality of life. Gene therapy may become available in the future.
Activity is encouraged. Inactivity (such as bedrest) can worsen the muscle disease. Physical therapy may be helpful to maintain muscle strength and function. Orthopedic appliances (such as braces and wheelchairs) may improve mobility and the ability to care for yourself.
Expectations (prognosis)
Duchenne muscular dystrophy leads to quickly worsening disability. Death usually occurs by age 25, typically from lung disorders.
Complications
Cardiomyopathy
Congestive heart failure (rare)
Deformities
Heart arrhythmias (rare)
Mental impairment (varies, usually minimal)
Permanent, progressive disability
Decreased mobility
Decreased ability to care for self
Pneumonia or other respiratory infections
Respiratory failure
