STUDY TITLE: Insights into the genetic basis of retinal detachment
SUMMARY: Identification of 11 genetic variants associated with retinal detachment.
OVERVIEW: The retina is a thin layer of cells in the back of the eye that detects light and enables vision. Retinal detachment is a serious medical condition that occurs when the retina is pulled away from its normal position and damaged in the process. If the condition is not immediately treated it can result in permanent blindness. Though common, genetic predisposition to this condition is not well understood. To determine genetic risk factors for this condition, this study analyzed the genomes of over 5,000 individuals of European ancestry who suffered from detachment. The study discovered 11 genetic variants associated with the condition. Multiple variants have been previously linked to other eye conditions including macular degeneration, nearsightedness, and glaucoma.
DID YOU KNOW? Because retinal detachment can be caused by external eye injuries, it is recommended to wear safety glasses during potentially hazardous activities. Typical symptoms of the condition are blurry vision, the sudden appearance of floaters and flashes of light. [SOURCE]
SAMPLE RESULTS: Learn more about the Nebula Research Library.
DETACHMENT-ASSOCIATED VARIANTS: rs10765567, rs74764079, rs1042602, rs4373767, rs11992725, rs11187838, rs1248634, rs11217712, rs4243042, rs7940691, rs9651980
ADDITIONAL RESOURCES:
Retinal detachment (Video)
WEEKLY UPDATE: December 26, 2019
