11-beta-hydroxylase deficiency (11B-OHD) is part of a family of disorders called congenital adrenal hyperplasia (CAH), which disrupt hormone production and sexual development and maturation.
11B-OHD CAH affects the function of the adrenal glands, which produce hormones that regulate many essential functions in the body. In individuals with 11B-OHD CAH, the adrenal glands produce excess androgens (male sex hormones).
There are two types of 11B-OHD: classic and non-classic. From birth, females with the classic type of 11B-OHD usually have ambiguous genitalia. Males with the classic type of 11B-OHD are typically born with male genitalia. Both males and females with the classic type can have early puberty, decreased fertility, short stature in adulthood, abnormal levels of sodium and potassium in the blood, and high blood pressure starting in childhood.
In the non-classic type of 11B-OHD, both males and females are born with typical genitals. Females with the non-classic type may experience irregular periods, decreased fertility, and excess hair growth on the face and body. Males with the non-classic type can have short stature.
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.
11-beta-hydroxylase-deficient congenital adrenal hyperplasia 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 11-beta-hydroxylase-deficient congenital adrenal hyperplasia, there’s a one in four chance that their children could develop symptoms.
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 11-beta-hydroxylase-deficient congenital adrenal hyperplasia, 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
The biggest benefit of screening for 11-beta-hydroxylase-deficient congenital adrenal hyperplasia 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 11-beta-hydroxylase-deficient congenital adrenal hyperplasia 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.