eugenelabs logo Back to condition list

Joubert syndrome and related disorders (RPGRIP1L related)

RPGRIP1L-related disorders (RRD) include Joubert syndrome 7, COACH syndrome and Meckel syndrome 5. They are a group of conditions which affect many parts of the body, caused by changes in the RPGRIP1L gene. Symptoms can include brain abnormalities, rapid breathing, weak muscle tone, vision problems, intellectual disability, and movement and coordination problems. Seizures and liver or kidney problems are also common.

Symptoms can vary, even in the same family. Life expectancy can be limited depending on the severity of symptoms for affected individuals. Early initiation of treatment is recommended to help optimise outcomes.

Quick facts about Joubert syndrome and related disorders (RPGRIP1L related)
Genes: RPGRIP1L
Inheritance: Autosomal Recessive
Alternative Names: Joubert syndrome type 7, COACH syndrome, Meckel syndrome type 5
Relevant resources for Joubert syndrome and related disorders (RPGRIP1L related)

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 Joubert syndrome and related disorders (RPGRIP1L related) inherited?

Joubert syndrome and related disorders (RPGRIP1L 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 Joubert syndrome and related disorders (RPGRIP1L 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 Joubert syndrome and related disorders (RPGRIP1L 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 Joubert syndrome and related disorders (RPGRIP1L related) before or early in pregnancy?

The biggest benefit of screening for Joubert syndrome and related disorders (RPGRIP1L 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 Joubert syndrome and related disorders (RPGRIP1L 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.