Starting a family is a thrilling milestone.
One important step in this journey is understanding any genetic health risks that might affect your child. NxGen MDx carrier screening offers prospective parents a deeper look into their genetic health, assessing the potential of passing on hereditary conditions like cystic fibrosis or fragile X syndrome.
What Is Carrier Screening?
Carrier screening is a genetic test that checks for genes associated with certain conditions. Most carriers of these genes are healthy and don’t experience symptoms. However, if both partners carry the same autosomal recessive condition, there’s a 25% chance that their child may inherit it. In the case of X-linked conditions, if the mother is a carrier, male children have a 50% chance of inheriting the condition.
Why Opt for Carrier Screening?
Even without a family history of genetic conditions, there’s still a possibility of risk. In fact, around 80% of babies with genetic conditions are born to families with no known history. Carrier screening before or during pregnancy can help families:
- Gain insight into any potential health risks for their child
- Plan preconception and pregnancy care more effectively
- Select appropriate healthcare providers and birth support
- Access early diagnosis and treatment options
- Make well-informed reproductive choices
Building a Healthier Future with Knowledge
Carrier screening allows you to make informed choices for your family’s health and future. By understanding possible genetic risks, you can take proactive steps to prepare for a safe and healthy journey into parenthood. Click here to locate a NxGen MDx carrier screening provider in your area.
