Table 1. Blind subject group details.
| Group | Age / Sex | Blindness onset | Acuity | Cause |
|---|---|---|---|---|
| Congenital | 28 M | 0 | NLP | anophthalmia (OTX2 mutation) |
| Congenital | 31 F | 0 | NLP | Isolated bilateral anophthalmia |
| Congenital | 18 M | 0 | NLP | Isolated bilateral anophthalmia |
| Congenital | 20 F | 0 | NLP | Isolated bilateral anophthalmia |
| Congenital | 23 M | 0 | NLP | Isolated bilateral anophthalmia |
| Congenital | 25 M | 0 | NLP | Isolated bilateral anophthalmia |
| Congenital | 37 M | 0 | LP | ROP |
| Congenital | 59 M | 0 | NLP | ROP |
| Congenital | 64 F | 0 | NLP | Congenital optic atrophy |
| Congenital | 58 M | 0 | NLP | ROP |
| Congenital | 33 F | 0 | LP | Congenital hypoplasia |
| Congenital | 51 M | 0 | LP | Cataracts |
| Congenital | 58 F | 0 | NLP | ROP |
| Congenital | 54 F | 0 | NLP | ROP |
| Congenital | 63 F | 0 | NLP | Congenital optic atrophy |
| Congenital | 53 F | 0 | NLP | ROP |
| Congenital | 62 M | 0 | LP | Cataracts, glaucoma |
| Congenital | 62 F | 0 | LP | ROP |
| Congenital | 56 F | 0 | NLP | Retrolental fibroplasia |
| Congenital | 69 M | 0 | NLP | Glaucoma |
| Congenital | 61 F | 0 | LP | Optic atrophy |
| Congenital | 30 F | 0 | NLP | Microophthalmia |
| Congenital | 32 F | 0 | NLP | ROP |
| Congenital | 65 M | 0 | NLP | Leber congenital amaurosis |
| Congenital | 57 F | 0 | NLP | ROP |
| Congenital | 48 F | 0 | NLP | ROP, glaucoma, vitreous hemorrhage, cataracts |
| Congenital | 23 F | 0 | LP | Congenital cataracts, glaucoma |
| Congenital | 19 M | 0 | - | Leber congenital amaurosis |
| Congenital | 23 M | 0 | - | Leber congenital amaurosis |
| Congenital | 19 F | 0 | - | Leber congenital amaurosis |
| Congenital | 19 M | 0 | - | Leber congenital amaurosis |
| Congenital | 23 F | 0 | - | Leber congenital amaurosis |
| Congenital | 21 F | 0 | - | Leber congenital amaurosis |
| Congenital | 34 F | 0 | - | Leber congenital amaurosis |
| Congenital | 52 M | 0 | - | Leber congenital amaurosis |
| Congenital | 28 F | 0 | - | Leber congenital amaurosis |
| Congenital | 22 F | 0 | - | Leber congenital amaurosis |
| Congenital | 20 F | 0 | - | Leber congenital amaurosis |
| Congenital | 17 M | 0 | - | Leber congenital amaurosis |
| Congenital | 48 M | 0 | - | Leber congenital amaurosis |
| Postnatal | 62 F | 4 | NLP | Trauma |
| Postnatal | 69 F | 7 | LP | Cone-Rod Dystrophy |
| Postnatal | 55 F | 8 | NLP | Uveitis |
| Postnatal | 46 F | 8 | LP | Retinitis pigmentosa |
| Postnatal | 48 M | 12 | NLP | Trauma |
| Postnatal | 69 F | 13 | LP | Juvenile macular degeneration |
| Postnatal | 58 F | 14 | NLP | “Eye tumors at birth” |
| Postnatal | 53 M | 25 | LP | Ocular infection |
| Postnatal | 59 M | 28 | NLP | Diabetic (Type 1) Retinopathy |
| Postnatal | 58 M | 29 | NLP | Congenital cataract, retinal detachment |
| Postnatal | 72 M | 35 | LP | Retinitis pigmentosa |
| Postnatal | 40 M | 36 | LP | Glaucoma, cataracts |
| Postnatal | 62 F | 40 | LP | Retinitis pigmentosa |
Age at blindness onset given in years. ROP—Retinopathy of Prematurity; NLP—No light perception; LP—Light perception. Values unavailable for some subjects.