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Muscular Dystrophy Treatment

Muscular Dystrophy

Muscular dystrophies (MD) are a group of genetically inherited conditions that cause progressive muscle weakness and loss of muscle mass (wasting). It may affect one muscle group first and spread over time.

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Symptoms

Falling often
Waddling gait
Enlarged calf muscles
A curved spine (scoliosis)
Stiff muscles and muscle pain
Swallowing or breathing problems
Difficulty walking, running or jumping

Other signs include learning difficulties, delayed growth, or heart problems, such as arrhythmia and heart failure.

Types

Common types of MD include Duchenne (DMD), Becker (BMD), facioscapulohumeral (FMD), myotonic dystrophy, congenital (CMD) and limb-girdle (LGMD). Duchenne is the most common type and often affects boys.
Diagnosis

We will perform a physical exam, blood or enzyme tests, electromyography (EMG) and a muscle biopsy to diagnose MD. You might also need heart and lung monitoring tests to check the function of these organs.
Treatment

Treatments include medication, physical and occupational therapies, mobility aids, braces, and surgery. You might also need respiratory care if your lungs are affected, such as using a sleep apnoea device. People with MD often benefit from joining support groups to manage their emotional health and speak to others who can relate.

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Ten Harley Street Limited
10 Harley Street
London W1G 9PF
United Kingdom

Opening Hours:
Monday to Friday 9am to 5pm

Call: 07954 847 479