Genetic Premarital Screening

Genetic premarital screening is a scientific, informed step that helps both partners understand their genetic compatibility and confirm the likelihood of passing hereditary diseases on to future children.

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How does genetic premarital screening detect hereditary disease risks for future generations?

Through genetic premarital screening, a number of genes linked to common hereditary diseases are analyzed, such as thalassemia, sickle cell anemia, cystic fibrosis, and certain metabolic disorders. The analysis shows whether one partner (or both) carries a genetic mutation that may be passed on to the next generation, even if they currently show no symptoms.

Why genetic premarital screening is an essential step

This screening is a necessary, comprehensive option, especially for those who want to build a healthy family from the start. It enables informed, early decisions, such as seeking medical consultations or considering well-planned reproductive options, including assisted reproduction or preimplantation genetic diagnosis, if risks are present.

How many times do you need to do genetic premarital testing?

What sets genetic premarital testing apart is that it is done only once in a lifetime and is considered a permanent source of information, enabling you to move forward toward a stable married life, free from anxiety about your children’s future health.

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