Duchenne Muscular Dystrophy

Muscular dystrophy has several forms.1 Duchenne muscular dystrophy (DMD) is the most common, accounting for over 50% of all cases.1 If you would like to know more about this particular form of muscular dystrophy, you can read information here on the causes and effects of DMD, how and when it typically progresses, and what this means in the longer term for people with DMD.

We will take a look at a protein called dystrophin and explain how mutations in the gene for this important molecule affect the muscles of the body. We talk about how, and where, these mutations happen in the pathway to having a baby.

The information in these articles covers how it is that some people can be carriers without showing signs of having a faulty gene but can pass the gene on to the next generation, and the likelihood of the gene being passed on further in each pregnancy. You can also find out why it is so rare for girls to develop DMD and why only women can be carriers. We discuss what it means to be a carrier, and how regular monitoring is important for all carriers as in some cases carriers may show some signs of disease requiring treatment.

  1. National Institutes of Health. What are the types and symptoms of muscular dystrophy (MD)? Available at https://www.nichd.nih.gov/health/topics/musculardys/conditioninfo/types [last accessed March 2021].
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Muscular dystrophy
Neuromuscular disorders
Genetics & inheritance
Duchenne Carriers
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Being aware of developmental milestones is an important consideration for your child’s health. While developmental delay may be nothing to worry about, it can sometimes be a sign of a muscle disorder

Understanding Duchenne: Duchenne muscular dystrophy: what you need to know

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Causes of Duchenne: What causes Duchenne? The importance of dystrophin

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Duchenne inheritance: What does it mean to be a carrier of Duchenne?

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What is the genetic cause of Duchenne muscular dystrophy?

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Duchenne inheritance: How is Duchenne passed through families?

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