Derniers ajouts - Retina Gallery ~ Full Sized Retina Images

Derniers ajouts - Dystrophies

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 146 fois58-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 OU06 Janvier 2024

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 158 fois58-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 OU06 Janvier 2024

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 141 fois58-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 OU06 Janvier 2024

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 156 fois58-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 OU06 Janvier 2024

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 145 fois58-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 OU06 Janvier 2024

Bietti's Crystalline Dystrophy - CYP4V2 homozygousvu 173 fois58-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 OU06 Janvier 2024

Leber's congenital amaurosisvu 248 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 236 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 225 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 210 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 222 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 240 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 210 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 223 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 236 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 211 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 253 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 235 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 202 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 176 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Leber's congenital amaurosisvu 242 fois4 year old child with nystagmus and no evidence of fixation. Genetic testing showed LCA 922 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 206 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 166 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 193 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 189 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 200 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Gyrate atrophy vs Myopic Degenerationvu 198 fois73 year old female with VA 20/16 OD 20/32 OS. Has cnvm in the left eye. Genetic testing for gyrate atrophy was negative.16 Septembre 2023

Usher Syndrome - USH2Avu 315 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 338 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 349 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 248 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 256 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 258 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 262 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

Usher Syndrome - USH2Avu 229 fois23 year old female Extended HPI: Vision trouble for about five years. She has some trouble with night vision and was told that her retina looked abnormal. There are no family members that are known to have an inherited retinal disease.
Medical Hx: Sensorial Neural Hearing Loss. Chorionic migranes.
Systemic Meds: None.
VA 20/32 OD, 20/25 OS
Color vision normal

Heterozygous for USH2A pathological mutation and for an USH2A VUS16 Juillet 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 220 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 200 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 201 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 249 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 245 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 262 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 226 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 238 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 259 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 241 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 227 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 230 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 229 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 234 foisShe 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:2119 Mars 2023

25 year old with Stargard and 2 ABCA4 mutations.vu 236 foisShe 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:2119 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 240 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 237 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 268 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 245 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 235 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 272 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 221 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 211 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 187 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 202 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 225 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 191 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 208 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 249 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 213 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 198 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 277 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 227 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 200 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 244 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 201 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 194 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 220 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 250 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 259 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 238 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 216 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 195 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 263 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 232 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 210 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 233 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 209 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 215 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

Stargardt Disease - Very Mild - 24 year oldvu 229 foisThis patient has 3 different ABCA4 mutations. His mother and sister have stargardts and his father has RP. His sisters images are also on Retinagallery.com19 Mars 2023

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