Additional file 1 of Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia

Additional file 1: Table S1. The gene list of the ophthalmic targeted exome sequencing panel included 736 genes. Table S2. Clinical phenotype and molecular diagnosis of 75 patients with unilateral high myopia. Table S3-1. The distribution of peripheral fundus findings in unilateral high myopia children. Table S3-2. The distribution of peripheral fundus findings in 20 unilateral high myopia children with genetic defects. Table S3-3. The distribution of peripheral fundus findings in unilateral high myopia children with or without genetic defects. Table S4. Comparison of baseline characteristics between groups with and without genetic defects. Table S5. The follow-up study of refraction in patients with unilateral high myopia in this study.