Post-marriage genetic screening

Post-marriage genetic screening helps couples assess the likelihood of passing hereditary diseases to children and provides preventive and medical options based on accurate results.

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Assessing hereditary risk for children

Through post-marriage genetic screening, the genes of both spouses are analyzed to confirm the presence or absence of genetic mutations linked to serious or chronic hereditary diseases. This test is used to determine whether there is a real risk of passing mutations to children, allowing couples to prepare early or consult genetic medicine specialists to make decisions based on accurate data.

Protecting children from hereditary diseases

The test is especially useful for couples with a family history of hereditary diseases, in cases of consanguineous marriage, or even for those who have previously had an affected child. It is also an important support tool for those seeking to use techniques such as IVF or preconception genetic diagnosis.

How often do you need to do post-marriage genetic screening?

The best thing about post-marriage genetic screening is that it is done only once in a lifetime, giving you clear knowledge that helps you move forward with confidence toward building a healthy family. The test does not require complex procedures; it is a simple step, yet one with a profound impact on the family’s future and children’s health.

Make awareness part of your parenting journey, and make the right decision from the start with post-marriage genetic screening – because fatherhood and motherhood begin with responsibility.

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