Genetic conditions are diseases that can be passed from parents to children. Some conditions may be inherited if only one parent has the changed gene, while others can be inherited only if both parents have the changed gene.
If one or both parents have a gene change (mutation) or have a genetic condition, the risk of passing the condition on to a child is the same with each pregnancy. Having one healthy or one affected child doesn't change the odds that future children will or will not be affected.
If the baby's mother or father or anyone in either of their families has a genetic condition, genetic counseling may help the family decide what type of prenatal testing they want.
Genetic conditions that may be inherited include:
A small number of conditions occur because of a one-time mistake in a single gene (new mutation), such as a change in a gene of one of the parents' egg or sperm cells or because of a change in a gene of the fetus. These one-time genetic changes are unlikely to happen again in future pregnancies.
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How do you tell others that your baby has a genetic condition?
A challenge parents may face is how to tell family members and friends about their child's condition. If you don't learn that your baby has a genetic condition until after your baby is born, you will have little time to absorb the information before you need to answer questions from excited family and friends who are eager for news.
The best approach may be to simply state the facts. You could say something like, "Our baby was diagnosed with a genetic condition." If you aren't ready to talk about your child's condition beyond that, say so. You may feel able to tell only one or two people. If this is the case, think about asking them to share the news with others. There is no right or wrong way to tell people. Know that there are resources to help you.