Abu Dhabi Genome Expert on Hereditary Eye Detection
The article focused on the efforts of the Abu Dhabi Department of Health in utilizing genomics to facilitate early detection of hereditary eye diseases. A study conducted in partnership between the Department and M42 revealed that the screenings encompassed 329 genes linked to genetic retinal diseases, analyzing data from over 500,000 Emirati citizens, making it one of the largest studies worldwide. The results identified approximately 100 genetic causes associated with inherited vision loss, clarifying that the presence of a genetic mutation does not necessarily guarantee the development of the disease. This enhances diagnostic accuracy and contributes to early intervention and preventive treatment by linking the data to health records on the "Malafi" platform. These initiatives align with Abu Dhabi's vision of building a preventive healthcare system based on prediction and early intervention, with a focus on applying genomics to improve patients’ lives and reduce cases of hereditary vision loss.
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