Juvenile hemochromatosis

Hereditary Hemochromatosis (HH) is a common and highly variable genetic condition that causes the body to store too much iron from the diet. Early symptoms may include fatigue, abdominal pain and joint aches and is more commonly seen in childhood or early adult years.

Early symptoms can often be missed, however ‘iron overload’ can build up in various parts of the body and can cause long term damage to organs such as the liver, heart, pancreas, joints and sex organs.

If left untreated, it can lead to early death; but if diagnosed early, Hereditary Hemochromatosis can be treated and managed effectively with no impact on life quality or expectancy. Treatment can include having blood drawn on a regular basis to lower iron levels.

Quick facts about juvenile hemochromatosis
Genes: HJV
Inheritance: Autosomal Recessive
Relevant resources for juvenile hemochromatosis

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 juvenile hemochromatosis inherited?

juvenile hemochromatosis 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 juvenile hemochromatosis, 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 juvenile hemochromatosis, 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 juvenile hemochromatosis before or early in pregnancy?

The biggest benefit of screening for juvenile hemochromatosis 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 juvenile hemochromatosis 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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