eugenelabs logo Back to condition list

Congenital disorder of glycosylation (SLC35A3-related)

Congenital disorder of glycosylation (CDG) are a group of conditions caused by several genes, one of which is SLC35A3. People born with SLC35A3-related CDG usually present with skeletal changes, such as joint deformities that restrict movement in the hands and feet (arthrogryposis) and dislocation of their knees or hips. They may also experience intellectual disability, autism spectrum disorder, seizures, poor muscle tone (hypotonia) and a small head, chin, and jaw. Treatment is focused on managing the individual's symptoms.

Quick facts about congenital disorder of glycosylation (SLC35A3-related)
Genes: SLC35A3
Inheritance: Autosomal Recessive

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.

Learn more about genetics

How is congenital disorder of glycosylation (SLC35A3-related) inherited?

congenital disorder of glycosylation (SLC35A3-related) 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 condition.

If both parents are carriers of congenital disorder of glycosylation (SLC35A3-related), there's a one in four chance that their children could develop symptoms.

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 condition in your child. Eugene offers an inclusive genetic carrier screening panel that includes congenital disorder of glycosylation (SLC35A3-related), 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.

Learn more about carrier screening

Should parents screen for congenital disorder of glycosylation (SLC35A3-related) before or early in pregnancy?

The biggest benefit of screening for congenital disorder of glycosylation (SLC35A3-related) 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 condition is low.

Since 90% of children that have a recessive genetic condition like congenital disorder of glycosylation (SLC35A3-related) 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 condition in the first place.