Primary hyperoxaluria type 3

Primary hyperoxaluria type 3 (PH3) is a condition that causes the body to produce too much oxalate (oxalic acid). The extra oxalate combines with calcium to cause kidney stones, which can eventually lead to kidney damage and kidney failure. Damage to other organs, including bones and blood vessels, may also occur.

Symptoms usually present in childhood, although age of onset may vary. Without treatment, kidney damage is progressive and in severe cases can be fatal by middle age. The impact of this disease is influenced by the extent of kidney disease and the response to treatments, and may require kidney transplant.

Quick facts about primary hyperoxaluria type 3
Genes: HOGA1
Inheritance: Autosomal Recessive
Relevant resources for primary hyperoxaluria type 3

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 primary hyperoxaluria type 3 inherited?

primary hyperoxaluria type 3 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 primary hyperoxaluria type 3, there’s a one in four chance that their children could develop symptoms.
Learn more about carrier screening

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 primary hyperoxaluria type 3, 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 primary hyperoxaluria type 3 before or early in pregnancy?

The biggest benefit of screening for primary hyperoxaluria type 3 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 primary hyperoxaluria type 3 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.

Wondering if this test is right for you?

Take a two minute quiz to find out.