A: Comparisons of the phenotypes between patients in our study and previous studies (STL1, ocular-only STL, STL2, and Marshall Syndrome). B: Comparisons of the phenotypes between children and adults with eoHM harboring STL mutations. VO, vitreous opacity; RD, retinal detachment; HL, hearing loss; Skel, skeletal abnormality; HJ, joint hypermobility. To access the data, click or select the words “Appendix 1.”