What is Becker's Muscular Dystrophy?

Written by Medicover Team and Medically Reviewed by Dr K Suresh , Neurologist


Becker's Muscular Dystrophy (BMD) is a rare genetic condition that causes muscles to slowly weaken over time. It mostly affects boys and young men, often starting in the teenage years. The condition makes it harder for muscles to repair themselves after regular use.

Unlike Duchenne muscular dystrophy, which is more severe and starts earlier, BMD has a slower progression. Many people with BMD stay active into adulthood and may not need a wheelchair until later in life. Early diagnosis and proper care can help manage symptoms and maintain mobility longer.

What Are the Symptoms of Becker's Muscular Dystrophy?

The symptoms of BMD usually appear between the ages of 5 and 15 but may show up later. The muscles in the hips, thighs, and shoulders are usually affected first. Over time, the heart and breathing muscles may also weaken.

Common symptoms include

  • Difficulty climbing stairs or getting up from the floor
  • Frequent falls or trouble running
  • Enlarged calf muscles (muscle tissue is replaced with fat)
  • Fatigue after mild exercise
  • Walking on toes or with a waddling gait
  • Muscle cramps or stiffness
  • Weakness in the arms and legs that gets worse with time

Some people also develop learning problems or mild heart issues.


What Causes Becker's Muscular Dystrophy?

Becker's Muscular Dystrophy is caused by a change (mutation) in the dystrophin gene. This gene helps make a protein called dystrophin, which is needed for muscle strength and repair. In BMD, the body makes some dystrophin, but it is either not enough or not working properly.

Key facts about the cause

  • Passed from mother to son (X-linked recessive inheritance)
  • Only males usually show symptoms
  • Females can be carriers and may have mild muscle weakness or heart issues

Genetic testing can confirm the presence of the gene mutation.


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How Is Becker's Muscular Dystrophy Diagnosed?

Diagnosing BMD involves a mix of physical exams, blood tests, and muscle studies. Since early symptoms can look like other muscle problems, testing is important to make a clear diagnosis.

Diagnosis may include

  • Blood tests: Check for high levels of creatine kinase (CK), a sign of muscle damage
  • Genetic testing: Looks for changes in the dystrophin gene
  • Electromyography (EMG): Measures muscle activity
  • Muscle biopsy: Checks for dystrophin in the tissue
  • Heart tests: ECG or echocardiogram to monitor heart function

Early diagnosis helps with planning care and managing symptoms.


What Are the Treatment Options for Becker's Muscular Dystrophy?

There is no cure for BMD, but treatments can help slow the symptoms and improve daily life. A combination of therapies often works best.

Common treatment approaches

  • Physical therapy: Keeps muscles strong and flexible
  • Occupational therapy: Helps with everyday tasks and independence
  • Medications: Steroids may help slow muscle loss
  • Heart medications: Used if the heart is affected
  • Breathing support: Non-invasive machines if lung function weakens
  • Mobility aids: Braces, walkers, or wheelchairs if needed

Regular checkups with specialists help manage the condition as it changes.


Can Becker's Muscular Dystrophy Be Prevented?

BMD is a genetic condition, so it cannot be prevented. However, early testing in families with a history of muscular dystrophy can help detect the condition before symptoms appear.

Helpful prevention tips

  • Genetic counseling for families with known cases
  • Carrier testing for mothers and female relatives
  • Prenatal testing if desired during pregnancy

Managing symptoms early can help slow progression and improve quality of life.


When Should You See a Doctor?

If your child shows signs of muscle weakness or delays in walking, it's best to talk to a doctor. Early symptoms of BMD may look like other conditions, but should not be ignored.

Talk to a doctor if you notice

  • Trouble walking, running, or climbing stairs
  • Large calf muscles that feel firm
  • Walking on toes or muscle stiffness
  • A family history of muscular dystrophy

Early care can make a big difference in long-term health.


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What Is the Outlook for Becker's Muscular Dystrophy?

The outlook for BMD is better than for other types of muscular dystrophy. Most people can walk into their 30s or 40s. With good care, some stay mobile even longer. However, over time, muscle weakness and heart problems can affect daily life.

A strong care plan, regular monitoring, and emotional support can help individuals live full and active lives for many years.


Our Experience Treating Becker's Muscular Dystrophy at Medicover

At Medicover, we offer expert care for children and adults with Becker's Muscular Dystrophy. Our neurology team works with heart, lung, and rehab specialists to create a complete care plan for every stage of the condition.

We provide

  • Advanced genetic testing and early diagnosis
  • Ongoing physical and respiratory therapy
  • Custom treatment plans based on age and need
  • Support for families, including counseling and education
  • Long-term monitoring of heart and lung health

We focus on helping each person live as independently and comfortably as possible.


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Frequently Asked Questions

Variations in the dystrophin gene can affect heart muscle differently. Some mutations target skeletal muscle more than cardiac tissue.

Light exercise may help maintain mobility early on, but overexertion can accelerate muscle damage. Supervised therapy is key.

Hormonal changes can increase muscle demands, and boys may first show faster decline in strength during or after puberty.

Yes, female carriers may develop mild symptoms like muscle cramps or cardiomyopathy due to skewed X-chromosome inactivation.

While less common, advanced stages may involve facial or speech muscles due to widespread muscle weakening.

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