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Leber's congenital amaurosisvista 232 veces4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 9
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Stargardt Disease - Very Mild - 24 year oldvista 231 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 230 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Leber's congenital amaurosisvista 230 veces4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 9
|
|
Stargardt Disease - Very Mild - 24 year oldvista 228 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 228 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 228 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 228 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 226 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Leber's congenital amaurosisvista 226 veces4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 9
|
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Stargardt Disease - Very Mild - 24 year oldvista 225 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 222 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 219 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Stargardt Disease - Very Mild - 24 year oldvista 219 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Stargardt Disease - Very Mild - 24 year oldvista 218 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 218 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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25 year old with Stargard and 2 ABCA4 mutations.vista 218 vecesShe has worn glasses since she was a kid. Since she became an adult her vision started to deteriorate more rapidly. This seems to have been happening since she entered the accounting department for the last two years. Her vision is worse in the light especially when she is driving. She can see green lights in the night but not in the day. She sees better on a dark background than on a light background. Her mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: Dcc20/160-1 PH20/80 Ncc20/200-2
VA OS: Dcc20/160-2 PH20/80-1 Ncc20/200-1
IOP: TP: OD:20 OS:21
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Leber's congenital amaurosisvista 217 veces4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 9
|
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Stargardt Disease - Very Mild - 24 year oldvista 216 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Gyrate atrophy vs Myopic Degenerationvista 215 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Gyrate atrophy vs Myopic Degenerationvista 213 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Stargardt Disease - Very Mild - 24 year oldvista 212 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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Stargardt Disease - Very Mild - 24 year oldvista 211 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Gyrate atrophy vs Myopic Degenerationvista 209 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Gyrate atrophy vs Myopic Degenerationvista 209 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Gyrate atrophy vs Myopic Degenerationvista 209 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Stargardt Disease - Very Mild - 24 year oldvista 208 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
|
25 year old with Stargard and 2 ABCA4 mutations.vista 208 vecesShe has worn glasses since she was a kid. Since she became an adult her vision started to deteriorate more rapidly. This seems to have been happening since she entered the accounting department for the last two years. Her vision is worse in the light especially when she is driving. She can see green lights in the night but not in the day. She sees better on a dark background than on a light background. Her mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: Dcc20/160-1 PH20/80 Ncc20/200-2
VA OS: Dcc20/160-2 PH20/80-1 Ncc20/200-1
IOP: TP: OD:20 OS:21
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Stargardt Disease - Very Mild - 24 year oldvista 206 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Stargardt Disease - Very Mild - 24 year oldvista 206 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 204 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
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|
Stargardt Disease - Very Mild - 24 year oldvista 202 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Stargardt Disease - Very Mild - 24 year oldvista 202 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
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|
Achromatopsiavista 202 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
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Stargardt Disease - Very Mild - 24 year oldvista 198 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
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Stargardt Disease - Very Mild - 24 year oldvista 197 vecesThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 193 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 191 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
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|
Leber's congenital amaurosisvista 190 veces4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 9
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 186 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 186 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 185 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Gyrate atrophy vs Myopic Degenerationvista 182 veces73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.
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Stargardt - Mother with Stargadts and father with RPvista 179 vecesHer mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: 20/160 OS: 20/160
She tested positive for ABCA4
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Pattern Dystrophy - PHPR2 Genevista 179 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
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Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 178 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 177 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Stargardt - Mother with Stargadts and father with RPvista 176 vecesHer mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: 20/160 OS: 20/160
She tested positive for ABCA4
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 174 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 172 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 171 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 171 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 171 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 171 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 169 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 167 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 167 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 166 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 165 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
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|
Pattern Dystrophy - PHPR2 Genevista 165 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 164 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 164 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Pattern Dystrophy - PHPR2 Genevista 164 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 163 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 163 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 163 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 162 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 161 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 161 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Pattern Dystrophy - PHPR2 Genevista 161 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 160 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Pattern Dystrophy - PHPR2 Genevista 160 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Pattern Dystrophy - PHPR2 Genevista 158 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 157 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 156 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 155 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Stargardt - Mother with Stargadts and father with RPvista 155 vecesHer mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: 20/160 OS: 20/160
She tested positive for ABCA4
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 154 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 154 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 153 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Stargardt - Mother with Stargadts and father with RPvista 153 vecesHer mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: 20/160 OS: 20/160
She tested positive for ABCA4
|
|
Pattern Dystrophy - PHPR2 Genevista 153 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
CRB1 Dystrophy - Inherited Retinal Disease - 14 year old malevista 153 vecesVision loss for 4 years OD 20/63, OS 20/160
|
|
Achromatopsiavista 152 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 152 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
CRB1 Dystrophy - Inherited Retinal Disease - 14 year old malevista 152 vecesVision loss for 4 years OD 20/63, OS 20/160
|
|
Achromatopsiavista 151 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 151 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 151 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 150 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Bietti's Crystalline Dystrophy - CYP4V2 homozygousvista 150 veces58-year-old-female (from Thailand)
Patient had evaluation for LASIK and there was concern that the BCVA was not normal.
PMHx Benign, Meds: none
VA 20/25 OU
|
|
Achromatopsiavista 150 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 150 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Stargardt - Mother with Stargadts and father with RPvista 149 vecesHer mom is genetically visually impaired with Stargardts. Her father has RP. The mother was genetically tested in Boston about 23 years ago. That was when the gene was first being isolated. (The mother has seven brothers and sisters and four have stargardts and they are legally blind. Also one cousin has it.)
VA OD: 20/160 OS: 20/160
She tested positive for ABCA4
|
|
Achromatopsiavista 148 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 148 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 146 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Pattern Dystrophy - PHPR2 Genevista 145 veces57 year old man- VA 20/25 OD, 20/20 OS - Many family members have retinitis pigmentosa
|
|
Achromatopsiavista 143 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
|
|
Achromatopsiavista 142 veces28 year old female Good vision since birth started wearing glasses at 2, denies trauma. She does have congenital nystagmus.
VA OD: Dcc20/200-2 PH20/200 NccJ7
VA OS: Dcc20/160 PHNI NccJ7
IOP: TP: OD:15 OS:12
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