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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: Ophthalmic Genet. 2016 Apr 6;38(1):98–100. doi: 10.3109/13816810.2015.1137328

Table 1.

Clinical Characteristics.

Patient Age Gender Diagnosis Mutation Best Corrected Visual Acuity
Right - Left
P1 49 Male X-linked Retinitis Pigmentosa RPGR 20/125 - 20/150
P2 19 Male X-linked Retinitis Pigmentosa RPGR 20/30 - 20/30
P3 29 Male X-linked Retinitis Pigmentosa RPGR 20/30 - 20/30-1
P4 50 Female Autosomal Dominant RP RHO 20/25 - 20/20
P5 15 Female Autosomal Dominant RP RHO 20/125 - 20/100
P6 43 Female Autosomal Dominant RP RHO 20/60 - 20/40
P7 60 Female Autosomal Dominant RP RHO 20/30 - 20/30
P8 47 Female Autosomal Recessive RP USH2A 20/20 - 20/40
P9 37 Female Autosomal Recessive RP USH2A 20/25 - 20/25
P10 46 Male Autosomal Recessive RP USH2A 20/20 - 20/20
P11 28 Male Autosomal Recessive RP USH2A 20/20 - 20/15
P12 65 Female RP/Usher Syndrome PRPF31 20/600 - 20/400
P13 72 Male Autosomal Recessive RP RDS/PRPH2 20/30 - 20/100
P14 24 Male Autosomal Recessive RP EYS 20/20 - 20/15
P15 8 Male Leber Congenital Amaurosis RPGRIP1 20/50 - 20/50
P16 31 Female Leber Congenital Amaurosis CRB1 20/200 - 20/200
P17 15 Male Leber Congenital Amaurosis CEP 290 20/40 - 20/50