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. 2013 Oct 9;33(41):16209–16219. doi: 10.1523/JNEUROSCI.0363-13.2013

Table 1.

Subject population demographicsa

ID Sex/age (yr)/handedness Age onset/severity (yr) Visual acuity Cause/notes
B01* F 33 L 0/0 LP Congenital hypoplasia
B03* F 32 R 0/18 NLP Retinopathy of prematurity (ROP)
B04* M 59 R 28/32 NLP Diabetic retinopathy
B05* F 23 R 0/18 LP Congenital cataracts, detached retinas
B06* F 48 0/20 NLP ROP; glaucoma; vitreous hemorrhage
B07* F 55 R 8/8 NLP Uveitis
B08* F 53 A 0/0 NLP ROP
B09* F 61 40/50 HM Retinitis pigmentosa (RP)
B10* M 58 R 0/0 NLP ROP
B12* F 46 R 8/8.5 NLP RP
B13* M 58 R 0/0 NLP ROP
B17* M 48 R 0/0 HM ROP
B02 F 69 R 7/7 HM Cone-rod dystrophy
B11 F 69 R 13/35 HM Juvenile macular degeneration
B14 F 62 R 0/0 NLP ROP
B15 M 40 R 36/36 HM Glaucoma (primary); cataracts (secondary)
B16 F 61 R 0/16 HM Optic atrophy
B18 M 50 R 0/0 HM Congenital cataracts
B19 M 53 R 20/35 HM Congenital infection
B20 F 63 R 54/56 NLP Diabetic retinopathy; detached retina
B21 M 69 R 0/15 NLP RP; glaucoma (secondary); detached retinas
B22 F 61 R 14/14 NLP Retinoblastoma; left eye blind at age of 3; right at 14
B23 M 48 R 12/12 NLP Trauma
B24 M 62 L 0/9 HM Congenital cataracts; glaucoma (secondary)
B25 F 69 R 0/0 NLP Congenital optic atrophy
S01* M 33 R
S06* M 41 R
S11* M 32 R
S13* F 58 R
S14* F 52 R
S15* F 46 R
S16* M 48 R
S17* F 68 R
S19* F 43 R
S20* F 51 R
S21* M 58 R
S22* F 44 R
S02 F 22 R
S03 M 25 A
S04 M 27 R
S05 F 25 R
S07 M 26 R
S08 F 22 R
S09 M 28 R
S10 F 22 R
S12 F 19 R
S18 F 24 R

aTwenty-five blind (B1–B25) and 22 sighted (S1–S22) individuals participated in the study. The blind population was heterogeneous with respect to age of onset and cause, although all had severe vision loss. R, Right-handed; L, left-handed; A, ambidextrous; NLP, no light perception; LP, best vision light perception only; HM, best vision hand-motion perception; —, missing value.

*Age-matched subgroups of 12 participants each.