Over 1,000 Emiratis benefit from mandatory pre-marital genetic testing in UAE
The initiative is a key part of the UAE's national efforts to prevent genetic disorders, reduce their spread, and promote healthier families across the country.
In a recent statement, EHS revealed that the genetic screening programme, which identifies potential genetic incompatibilities between couples, has already flagged 31 cases. These couples were given genetic counselling to help them make informed decisions about childbearing and pregnancy planning, ensuring they can proactively address potential health risks for their future children.
UAE Genome Programme
This testing initiative is also aligned with the broader objectives of the UAE Genome Programme and the National Genome Strategy. The programme seeks to establish a comprehensive genetic database of Emirati citizens, which will contribute to scientific research and shape future strategies for early medical interventions, thereby improving public health outcomes in the UAE.
What is genetic test
The genetic test, which is provided at EHS health centres, screens for the most prevalent genetic conditions affecting Emiratis. It examines 570 genes linked to more than 840 medical conditions, delivering accurate results quickly. This inclusion of genetic testing in pre-marital screenings marks a significant step toward strengthening the country's preventive healthcare initiatives and ensuring responsible family planning.
Where to go
Currently available at 22 health centres across various Emirates, the service is expected to expand in response to growing demand, ensuring better accessibility for all Emirati citizens. EHS is committed to enhancing service coverage to reach more individuals, empowering couples with the knowledge necessary for planning healthy families.
Why it matters
Premarital genetic testing is designed to protect public health by detecting potential health risks before marriage. It serves to identify genetic diseases, hereditary conditions, and other health concerns that may be passed to offspring, particularly in consanguineous marriages or when a family history of genetic disorders exists.
The screenings help reduce the incidence of serious congenital anomalies and inherited conditions like thalassaemia, sickle cell anaemia, G6PD deficiency, early-onset blindness, hearing impairments, and other conditions that can affect a child's physical and mental development. This proactive approach not only alleviates the psychological and emotional burden on families but also enables timely intervention, early diagnosis, and preventive care, which ultimately contributes to healthier future generations.
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