There are several genetic conditions that are more common in specific ethnic groups. The information below briefly reviews some general information about testing for these conditions. If you have questions about this information, please address them with the doctor during your scheduled appointment.
What are genes?
Genes are made up of DNA and are the codes or instructions that tell the body how to grow and develop. These genes are arranged on strings of information called chromosomes. We have two copies of each chromosome, one that is inherited from our mother and one that is inherited from our father; as a result, we have one copy of each gene.
What are recessive diseases?
Many conditions are now known to be caused by changes, or mutations, in genes. Some genetic conditions, known as recessive conditions, are caused when a change or mutation is present on both genes of a pair. This means that both the mother and father must pass on the same changed gene in order for a child to have a recessive condition.
What is a carrier?
A carrier is a person who has a change in only one gene of a pair and the other gene of the pair is working normally. A carrier is sometimes said to have the disease trait but has no physical symptoms of the disease. In many families, a recessive gene change or trait can be passed on through generations without ever being known. A recessive disease can only occur if a person who is a carrier has a baby with another person who is also a carrier. Such a couple would have a 1 in 4 (25 percent) chance, in each pregnancy, of having a baby with that recessive disease.
Who should be screened?
DNA tests are available to help a couple determine if they are carriers of the same recessive disease trait and are at risk for having children with that recessive condition. Some diseases occur more often in certain ethnic groups. Information about the carrier frequency of the more common recessive disease traits in certain ethnic groups is provided below. There are many other recessive conditions, not listed below, for which testing is not typically performed because the conditions are less common or because testing is not available.
|Sickle cell anemia||1/30-1/50|
|European Caucasian:||Cystic fibrosis||1/29|
|African American:||Sickle cell anemia||1/10|
How can I have carrier testing?
If you are interested in learning more about the genetic conditions more common in your specific ethnic group and the availability of carrier testing for these conditions, please ask our physician. You may also wish to check with your insurance company about whether this testing would be covered under your plan.
Hanabusa IVF is collaborating with Good Start Genetics to perform genetic carrier screening. Please visit their website to learn even more about this topic.