Factor IX deficiency (hemophilia B)

Factor IX deficiency (hemophilia B) is a bleeding disorder that causes individuals to bleed longer than others, due to a lack of a protein called coagulation factor IX, which helps the body form blood clots.

Due to this, people with this condition may experience prolonged bleeding following surgery, dental work, or injury. In more serious cases, spontaneous bleeding without injury may occur in the joints, muscles, and other organs. Milder cases may not be diagnosed until an affected individual experiences prolonged bleeding following an injury or surgery.

Factor IX deficiency is an X-linked condition and therefore, primarily affects males. Female carriers are not usually affected, though some may experience abnormal bleeding but it is typically milder than in males.

Quick facts about factor IX deficiency (hemophilia B)
Genes: F9
Inheritance: X-linked
Relevant resources for factor IX deficiency (hemophilia B)

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 factor IX deficiency (hemophilia B) inherited?

factor IX deficiency (hemophilia B) is an X-linked condition. X-linked conditions occur when there is a genetic variation on the X-chromosome. For these conditions, the sex of the parent who passes on the gene variation influences the risk for the children.

If the father is affected, all his daughters will have a variation on one of their X-chromosomes and be healthy carriers. Sons can only inherit these x-linked conditions from their mother and therefore, in this situation, will not be affected by the disease.

If the mother is a healthy carrier of an X-linked variation and has a son, there is a 50% chance that they could inherit this variant and be affected by the disease. If they have a daughter, there is a 50% chance that they will be a healthy carrier (just like her mum).

Another way of looking at this is that there is a 25% chance of having an affected son and a 75% chance that the child will not be affected by the disease.

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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 factor IX deficiency (hemophilia B), 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 factor IX deficiency (hemophilia B) before or early in pregnancy?

The biggest benefit of screening for factor IX deficiency (hemophilia B) 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.

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