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The prognosis for people with MD varies according to the type and progression of the disorder. Some cases may be mild and progress very slowly over a normal lifespan, while others produce severe muscle weakness, functional disability, and loss of the ability to walk.

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There is no cure for any form of muscular dystrophy. But medications and therapy can slow the course of the disease.

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Non-invasive prenatal diagnosis - safer testing avoids the risk of miscarriage

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Non-invasive prenatal diagnosis (NIPD) of genetic conditions avoids the risk of miscarriage. UCL researchers have led the implementation into clinical practice of NIPD for serious sex-linked and autosomal dominant disorders.

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Muscular Dystrophy is diagnosed through a physical exam, family medical history and tests

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1. - Pain in muscles

2. - abnormality walking

3. - muscle weakness

4. - loss of muscle

5. - permanent shortening of muscle

6. -delayed development or learning disability

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Muscular Dystrophy is  a group of genetic diseases that cause progressive weakness and loss of muscle mass.