The discovery of a new gene for blindness in children in China leads to defects in congenital eye tissue
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According to reports, congenital eye tissue defect is a serious blinding eye disease in children, there is a genetic predisposition, caused by the embryonic clot insufficiency 6-7 weeks, the disease is still lacking effective treatment. Peking University ophthalmologist Wang Lejin and Sichuan Provincial People's Hospital professor Yang Zhenglin have discovered a new cause of congenital eye tissue defects in the past 10 years in a Chinese congenital eye tissue defect family and 116 cases of sporadic cases. Gene - ABCB6.
The discovery of this gene is helpful for the detection of prenatal genes, avoiding the birth of children with such diseases, and laying a theoretical foundation for future gene therapy.