Genetics

At Dar Al-Baraa Medical Center, we understand the vital role of genetic health in family planning, fertility, and pregnancy care. Our Genetics Department offers advanced and comprehensive services to support couples and individuals at every stage of their journey towards conceiving and raising healthy babies. Led by pioneering experts in the field, we combine trusted medical expertise with the latest technology to provide accurate guidance and effective solutions. Whether you are planning to conceive, undergoing fertility treatments, or concerned about hereditary conditions, our specialists are here to guide you every step of the way.

1- Genetic Counseling (Online & In-Clinic)

We offer both online and in-person counseling, giving you the flexibility to receive professional advice in the way that suits you best. Our genetic experts review medical history, assess risks, and recommend personalized testing options.

Who can benefit from genetic counseling?

1. Couples planning to conceive a healthy baby.
2. Individuals or couples with a family history of genetic disorders.
3. Couples experiencing recurrent miscarriages without known causes.
4. Couples undergoing IVF treatment seeking to understand genetic risks.
5. Those interested in genetic screening for gender selection or fertility-related concerns.

What to expect:

• Risk assessment based on medical and family history.
• Guidance on advanced testing options such as PGT-A, NIPT, and premarital screening.
• Personalized recommendations to support informed decisions.

2- Preimplantation Genetic Testing (PGT-A)

PGT-A is an advanced screening test performed during IVF to detect chromosomal abnormalities in embryos before implantation. This significantly improves the chances of a successful pregnancy and reduces miscarriage risk.

Benefits of PGT-A:

• Identifies chromosomal abnormalities in embryos.
• Increases pregnancy success rates by selecting healthy embryos.
• Reduces the likelihood of miscarriages caused by chromosomal issues.
• Can support gender selection in family planning.

How it works:

1. Embryo biopsy performed in a controlled lab setting.
2. Embryos vitrified (frozen) while awaiting results.
3. Analysis with Next Generation Sequencing (NGS) to check all 23 chromosome pairs.
4. Healthy embryos selected, thawed, and transferred for implantation.

3- Non-Invasive Prenatal Test (NIPT)

The Non-Invasive Prenatal Test (NIPT) is a safe and highly accurate blood test available from the 10th week of pregnancy. It analyzes fragments of the baby’s DNA circulating in the mother’s blood to detect chromosomal conditions.

What NIPT screens for:

• Down syndrome (Trisomy 21)
• Edwards syndrome (Trisomy 18)
• Patau syndrome (Trisomy 13)
• Sex chromosome abnormalities
• Baby’s gender (optional)

Why choose NIPT?

• Non-invasive; only a blood sample is required, with no risk to the baby.
• Accuracy of over 99% for common conditions.
• Early detection that supports informed decision-making during pregnancy.
• NIPT is an essential step for expectant parents who want peace of mind and early reassurance about their baby’s genetic health.

4- Premarital & Pregnancy Genetic Testing

Premarital and prenatal genetic screening helps couples reduce the risk of passing on hereditary conditions to their children.
These tests are recommended for:

• Couples with a family history of genetic disorders.
• Couples with no clear family history but seeking precautionary reassurance.
• Couples planning IVF or assisted reproductive treatments.

By identifying potential genetic risks early, couples can take informed steps to ensure a healthier pregnancy and family future.

Schedule Your Consultation Today

To learn more about our genetic services or to schedule your online or in-clinic counseling session, contact us through our website or call our center. We’re here to guide you through every step of your journey to parenthood.