Genetic testing can help diagnose or confirm if your child has a genetic cardiovascular condition. It helps determine if a change in your child’s DNA explains the features of their heart anatomy or their risk for a cardiac condition that is seen in your family. Understanding the genetics of your child’s heart condition can help doctors determine the best treatment and care plan.
Most genetic tests require either a blood sample or a sample from a cheek swab or saliva. Sometimes a genetic test may also involve collecting samples from other family members, such as the child’s parents. There are two common categories of genetic testing in cardiovascular genetics:
Diagnostic genetic testing for a heart condition
This type of testing tries to identify the genetic change in your child that caused their cardiac condition or cardiac features. A confirmed genetic diagnosis allows your child’s cardiovascular care team to create a personalized treatment plan that focuses on that specific heart condition and other health or development concerns for which they may be at risk. If a genetic change is identified in your child, the clinical team can use this information to screen additional family members for the same genetic change to see if they carry the gene change and are at risk for developing the heart condition.
Predictive genetic testing for a heart condition
This type of testing is performed when someone in the family (such as a parent or sibling) has a known genetic change that puts other family members at risk for carrying the same genetic change and developing a cardiac condition. In this instance, predictive genetic testing is performed on a family member who is not known to be affected (asymptomatic) but is at risk for inheriting the known genetic change. If you have a genetic change that caused a cardiac condition, predictive testing will confirm if your child also has that genetic change and is at risk for developing the cardiac condition. It can also confirm if your child does not have the genetic change and is not at increased risk for developing the cardiac condition seen in the family.