Dysferlinopathy (including limb-girdle muscular dystrophy type 2B)

Dysferlinopathy is a group of muscle conditions caused by variants in the DYSF gene. People affected by dysferlinopathy experience muscle weakness that typically first appears in adolescence or young adulthood. The pattern of muscle weakness varies depending on the type of dysferlinopathy, however in most cases the weakness is progressive and many peolpe will require the assitance of a wheelchair.

Types of dysferlinopathy include limb-girdle muscular dystrophy type 2B (LGMD2B) which affects the pelvis and shoulders; miyoshi myopathy which tends to affect the lower legs; and scapuloperoneal syndrome which tends to affect the lower legs and shoulders.

Symptoms and severity of these conditions can vary, even between members of the same family. Treatment is focused on managing the individual's symptoms.

Quick facts about dysferlinopathy (including limb-girdle muscular dystrophy type 2B)
Genes: DYSF
Inheritance: Autosomal Recessive
Relevant resources for dysferlinopathy (including limb-girdle muscular dystrophy type 2B)

A quick genetics rundown

As humans we have about 23,000 genes. These genes are like tiny instruction manuals that influence our health, growth and development. We inherit half of our genes from our biological mum and the other half from our biological dad. These genes are lined up on structures called chromosomes. Most of us have 23 pairs of chromosomes. The first 22 pairs are called autosomes and for the most part - these are the same among men and women. The 23rd pair determine our sex - two X chromosomes for a female and one X and one Y chromosome for males.

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How is dysferlinopathy (including limb-girdle muscular dystrophy type 2B) inherited?

dysferlinopathy (including limb-girdle muscular dystrophy type 2B) is known as an autosomal recessive condition. For autosomal recessive conditions, if a person has a variation in one copy of their gene, they are a carrier. This means that they are healthy because they also have a working copy of the gene. But, they can still pass their non-working copy to their child.

If the other parent also happens to be a carrier of the same gene, there is a 25% (1 in 4) chance that they both pass this gene variation on to their child — and as such, have a child affected by the disease.

If both parents are carriers of dysferlinopathy (including limb-girdle muscular dystrophy type 2B), there’s a one in four chance that their children could develop symptoms.
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What is carrier screening?

Carrier testing is like a checkup for your genes. It tests to see if you carry a gene variation that could cause a serious genetic disease in your child. Eugene offers an inclusive genetic carrier screening panel that includes dysferlinopathy (including limb-girdle muscular dystrophy type 2B), but there's a total 301 conditions that can be tested.

Eugene’s carrier test is a clinical grade test that can be done from the comfort of your own home — it’s just a saliva test. You're also paired with a genetic counsellor who provides mindful support and guidance every step of the way.

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Should parents screen for dysferlinopathy (including limb-girdle muscular dystrophy type 2B) before or early in pregnancy?

The biggest benefit of screening for dysferlinopathy (including limb-girdle muscular dystrophy type 2B) is that it can help future parents understand their reproductive risk so they can be ready and empowered to make more informed decisions. If neither partner are carriers, it provides reassurance and peace of mind that the risk of having a child with a genetic disease is low.

Since 90% of children that have a recessive genetic disease like dysferlinopathy (including limb-girdle muscular dystrophy type 2B) had no previous family history of it, it often feels completely out of the blue for the parents. Getting screened is a way to know this risk in advance, which can help familes manage or even prevent the disease in the first place.

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