A Genetic Disorders Specialist and a member of the Kuwait Medical Genetics Center,
Know Your Doctor


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 Genetic Testing Services in Kuwait, including molecular genetic testing, cytogenetic analysis, and genetic diagnostics, to support couples and individuals at every stage of their journey toward conceiving and raising healthy babies.
Led by clinical genetics experts, we combine trusted medical expertise with the latest Next-Generation Sequencing (NGS) technology and advanced laboratory techniques to provide accurate guidance and effective solutions. Whether you are planning to conceive, undergoing fertility treatments, or concerned about hereditary conditions or congenital disorders, our specialists are here to provide personalized genetic care and support in reproductive genetics every step of the way.
We offer both online and in-person genomic counseling, giving you the flexibility to receive professional advice in the way that suits you best. Our genetic consultation services involve reviewing your medical history, assessing genetic risks, and recommending personalized testing options.
Couples planning to conceive a healthy baby
Individuals or couples with a family history of inherited disorders
Couples experiencing recurrent pregnancy loss without known causes
Couples undergoing IVF treatments seeking to understand fertility genetics and genetic risks
Those interested in carrier screening or advanced genetic testing for gender selection
Genetic risk assessment based on medical and family history
Guidance on advanced testing options such as PGT-A, pre-implantation test, NIPT, premarital screening, gene mutation screening, and chromosomal microarray analysis (CMA)
Personalized recommendations and genetic consultation services to support informed decisions
PGT-A / pre-implantation test is an advanced screening performed during IVF to detect chromosomal abnormalities in embryos before implantation. This significantly improves pregnancy success rates, reduces miscarriage risk, and contributes to the overall embryo genetic health.
Identifies chromosomal abnormalities in embryos
Increases pregnancy success rates by selecting healthy embryos
Reduces the likelihood of recurrent pregnancy loss caused by genetic issues
Can support gender selection in family planning
Embryo biopsy performed in a controlled laboratory setting
Embryos vitrified (frozen) while awaiting results
Analysis using Next-Generation Sequencing (NGS) technology to check all 23 chromosome pairs
Selection of healthy embryos ensures optimal embryo genetic health
The Non-Invasive Prenatal Test (NIPT) is a safe and highly accurate prenatal genetic screening 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 and gene mutations.
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Sex chromosome abnormalities
Baby’s gender (optional)
Non-invasive; only a blood sample is required, with no risk to the baby
Accuracy of over 99% for common conditions
Early detection supports informed decision-making during pregnancy
A vital step for expectant parents in Kuwait seeking peace of mind and reassurance about their baby’s genetic health
Premarital and prenatal genetic screening helps couples reduce the risk of passing on hereditary conditions, congenital disorders, and inherited diseases to their children.
Couples with a family history of hereditary disorders
Couples without a known 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. These tests may include carrier screening, chromosomal microarray analysis (CMA), and molecular genetic testing to provide comprehensive results.
Our department leverages state-of-the-art genetic diagnostics, including molecular genetic testing, cytogenetic analysis, and DNA sequencing, to support all stages of fertility genetics and reproductive genetics. These advanced tests ensure that patients in Kuwait receive accurate, evidence-based results for:
Inherited disorders detection
Chromosomal abnormalities
Gene mutation screening
Hereditary cancer risk evaluation
Personalized genetic consultation services
With personalized genetic care, we ensure that each couple or individual receives a tailored plan suited to their reproductive and family health goals.
To learn more about our comprehensive genetic services, or to schedule your online or in-clinic genomic 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, providing trusted genetic expertise and cutting-edge laboratory diagnostics to support healthy families.
Yes, even without a known family history, genetic counseling can help detect potential risks and offer peace of mind through precautionary testing.
A session typically lasts between 45 minutes to an hour, depending on your medical history and specific concerns.
The number of sessions depends on various factors, including your medical conditions, family history, and the results of the tests.
Both options offer the same level of expertise and care. Online counseling provides convenience, while in-clinic sessions offer face-to-face interaction.
Coverage varies by provider, so we recommend checking with your insurance company to determine whether genetic counseling and testing are covered under your plan.
Yes, your genetic information is strictly confidential. Only the patient who has signed the consent form will receive the results, ensuring privacy and security throughout the process.

A Genetic Disorders Specialist and a member of the Kuwait Medical Genetics Center,
Know Your Doctor