Carrier Screening
Carrier screening is a genetic test that can determine if you are a carrier of a genetic mutation for certain inherited diseases. Being a carrier means you have one copy of a gene mutation, but you may not have any symptoms of the disease. However, if both you and your partner are carriers for the same condition, there is a chance that your child could inherit the disease.
Why Carrier Screening is Important
Carrier screening can help you understand your risk of passing on an inherited condition to your children, allowing you to make informed decisions about your family planning options.
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