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. Author manuscript; available in PMC: 2017 Feb 21.
Published in final edited form as: Doc Ophthalmol. 2009 Nov 3;119(3):217–224. doi: 10.1007/s10633-009-9204-7

Table 1.

Subjects are separated by diagnosis

Diagnosis Subjects (n) D-FST eyes (n) FST2 eyes (n) Mean age (years) Median VA (logMAR) Mean rod ERG (Mv)
Normal 7 7 7 39.3 ± 13.8 0 ± 0.1 106.4 ± 18.4
Autosomal dominant retinitis pigmentosa 5 8 4 61.8 ± 12.8 0.9 ± 0.8 2.6 ± 5.8
Autosomal recessive retinitis pigmentosa 7 10 4 50.7 ± 12.2 1.1 ± 0.8 0
Isolate retinitis pigmentosa 9 10 4 56.4 ± 17.9 1.4 ± 0.8 0
X-linked retinitis pigmentosa 3 6 0 64.0 ± 4.0 1.4 ± 0.7 0
Leber congenital amaurosis 6 7 4 18.9 ± 9.7 1.6 ± 0.9 0
Usher syndrome 6 6 2 41.5 ± 9.9 0.6 ± 0.6 20.1 ± 49.2
Bardet–Biedl syndrome 2 2 0 43.5 ± 3.5 1.9 ± 0.2 0
Cone-rod dystrophy 4 4 3 47.3 ± 31.4 1.6 ± 0.4 15.6 ± 24.3

Number of patients per condition is listed with number of eyes tested per method. Mean age, median visual acuity and mean dark-adapted rod ERG amplitude are listed with standard deviations. Affected subjects with measureable ERGs met the visual field criteria. Values assigned for acuities unmeasurable by ETDRS vision chart were as follows: CF 1.7 logMAR, LP 2.0 logMAR and NLP 3.0 logMAR