Enimvaadatud - Dystrophies
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Choroidal Dystrophyvaatamisi: 602
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Posterior Polar Annular Choroidal Dystrophyvaatamisi: 60268 year old woman with know macular irregularities for over 20 years. She has since been followed another 6 years and her vision remains 20/25.
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vaatamisi: 601
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Retinitis Pigmentosa - Autosomal Dominant - Vision Loss at Young Age - Infraredvaatamisi: 600 54-year-old woman has autosomal dominant retinitis pigmentosa. Her mother and grandmother both had it and she has one son who has it and one daughter who doesn’t. She also has a sister with it. She lost vision since she was younger. She had cataract surgery done in January and February of this year. She has been seeing unusual flashing lights throughout the periphery and central vision for about the last year or two.
VISUAL ACUITY: OD 20/160, OS 20/160
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Non-specific (uncharaterized / unknown) Macular Dystrophy - ICGvaatamisi: 60059-year-old man has macular dystrophy in both eyes. He had some vision changes in medical school in the 1980s and saw Dr. Gass for that. He had some pigment epithelial irregularities in both eyes. He had strabismus as a child and had muscle surgery. He is color blind, along with many people in his family, and as far as he knows, it is congenital.
20/25, 20/30
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Fundus Albipunctatusvaatamisi: 60012 year old female with normal vision. She has 4 siblings all of whom have either white spots or spots on IR. Genetic testing by parents was deferred.
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Choroideremia - Adultvaatamisi: 60069 year old man with no family history of choroideremia and gradual vision loss in both eyes. VVA 20/125 OD; 20/63 OS
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Best Disease for 30 Years - 20/50 Vision both eyes - 61 Year Old Womanvaatamisi: 59961-year-old woman was diagnosed with Best’s disease about 30 years ago. She and her many family members were tested, both at the VA Hospital and then at USF. OD 20/50, OS 20/50
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 59955-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CMEvaatamisi: 5991 month of treatment with diamox 500 mg BID- cme is a little better
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Posterior Polar Annular Choroidal Dystrophyvaatamisi: 59868 year old woman with know macular irregularities for over 20 years. She has since been followed another 6 years and her vision remains 20/25.
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Stargart's Macular Dystrophy Severevaatamisi: 59732-year-old man carries a diagnosis of Stargardt’s disease with poor vision in both eyes since he was 13. He has not noticed any substantial change since he was here 4 years ago.
VISUAL ACUITY: OD 10/200, OS 8/200
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Congenital Achromatopsia vaatamisi: 59726-year-old man was diagnosed with congenital achromatopsia by ERG as a child. He has family members who also have this disorder. OD 20/200, OS 20/200.
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Late Onset Retinal Degeneration (L-ORD)vaatamisi: 59755 year old with acute vision loss from a CNVM in the right eye. He responded to Lucentis therapy. His mother and her family has been confirmed genetically to have L-ORD and were part of the early reports.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA LATEvaatamisi: 59646-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Posterior Polar Annular Choroidal Dystrophyvaatamisi: 59668 year old woman with know macular irregularities for over 20 years. She has since been followed another 6 years and her vision remains 20/25.
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Pigmented Peripheral Retinal Degenerationvaatamisi: 59642-year old male comes in for routine eye exam and to follow up on peripheral retinal degeneration in both eyes. VA is 20/20, right eye and 20/25, left eye. Patient is asymptomatic with no visual complaints.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA Earlyvaatamisi: 59546-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 595
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Fundus Albipunctatusvaatamisi: 59512 year old female with normal vision. She has 4 siblings all of whom have either white spots or spots on IR. Genetic testing by parents was deferred.
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vaatamisi: 594
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 59412-year-old had a dilated macular exam and the macula look abnormal. Interestingly, her mother, who is with her at this visit, was told about a year ago that her maculae are abnormal too. Her mother’s vision is fine. In the family tree, there are no known retinal dystrophies. They are both healthy.
VISUAL ACUITY: Her vision is 20/20 in both eyes.
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 594
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 59355-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa - Autosomal Dominant - Vision Loss at Young Age - Autofluorescencevaatamisi: 593 54-year-old woman has autosomal dominant retinitis pigmentosa. Her mother and grandmother both had it and she has one son who has it and one daughter who doesn’t. She also has a sister with it. She lost vision since she was younger. She had cataract surgery done in January and February of this year. She has been seeing unusual flashing lights throughout the periphery and central vision for about the last year or two.
VISUAL ACUITY: OD 20/160, OS 20/160
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Stargardt's Macular Dystrophy ABCA4 positivevaatamisi: 593Images show some progression over 3 years of macular dystrophy.
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 592Mothers macular photos
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X-linked Juvenille Retinoschisis - Peripheral Retinal Vascular Anomalies - Vitreous Hemorrhage - 8 Year Old Boyvaatamisi: 5928-year-old child OD 20/40, OS 20/50
OD: Vertical C/D ratio is 0.2. There are foveal cysts. There is also a retinal elevation inferiorly and there are patchy peripheral retinal hemorrhages.
OS: Vertical C/D ratio is 0.2. There are foveal cysts. There is peripheral retinal issues with some hemorrhage in some areas of peripheral retinoschisis.
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 592
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Congenital Achromatopsia vaatamisi: 59126-year-old man was diagnosed with congenital achromatopsia by ERG as a child. He has family members who also have this disorder. OD 20/200, OS 20/200.
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 59012-year-old had a dilated macular exam and the macula look abnormal. Interestingly, her mother, who is with her at this visit, was told about a year ago that her maculae are abnormal too. Her mother’s vision is fine. In the family tree, there are no known retinal dystrophies. They are both healthy.
VISUAL ACUITY: Her vision is 20/20 in both eyes.
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 59012-year-old had a dilated macular exam and the macula look abnormal. Interestingly, her mother, who is with her at this visit, was told about a year ago that her maculae are abnormal too. Her mother’s vision is fine. In the family tree, there are no known retinal dystrophies. They are both healthy.
VISUAL ACUITY: Her vision is 20/20 in both eyes.
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X-Linked Juvenille Retinoschisis 10 Year Old Child treated with Trusoptvaatamisi: 58810-year-old child has x-linked juvenile retinoschisis VA 20/60, OS is 20/100. Macula and Vision improved with Trusopt drops.
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 588
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 588
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Indocyanine Green Angiogram - Enhanced S Cone Syndrome - Goldmann Favre - vaatamisi: 58755-year-old woman while in college her vision was poor even with glasses and she sought evaluation for that. She was told after she had an electroretinogram at USF 15 years ago, that she had something with her blue cones. She does have poor night vision, but her reading vision is pretty good.
VISUAL ACUITY: OD 20/40, OS 20/40
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FAFvaatamisi: 58746-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Fundus Albipunctatusvaatamisi: 58712 year old female with normal vision. She has 4 siblings all of whom have either white spots or spots on IR. Genetic testing by parents was deferred.
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 58612-year-old had a dilated macular exam and the macula look abnormal. Interestingly, her mother, who is with her at this visit, was told about a year ago that her maculae are abnormal too. Her mother’s vision is fine. In the family tree, there are no known retinal dystrophies. They are both healthy.
VISUAL ACUITY: Her vision is 20/20 in both eyes.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA Earlyvaatamisi: 58646-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA Earlyvaatamisi: 58646-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 586
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Stargart's Macular Dystrophy Severe - New Vitreomacular Asymptomatic Vitreomacular Traction ODvaatamisi: 58532-year-old man carries a diagnosis of Stargardt’s disease with poor vision in both eyes since he was 13. He has not noticed any substantial change since he was here 4 years ago.
VISUAL ACUITY: OD 10/200, OS 8/200
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Best Disease for 30 Years - 20/50 Vision both eyes - 61 Year Old Womanvaatamisi: 58561-year-old woman was diagnosed with Best’s disease about 30 years ago. She and her many family members were tested, both at the VA Hospital and then at USF. OD 20/50, OS 20/50
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BESTS Diseasevaatamisi: 585
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vaatamisi: 584
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X-Linked Juvenille Retinoschisis 10 Year Old Child treated with Trusoptvaatamisi: 58310-year-old child has x-linked juvenile retinoschisis VA 20/60, OS is 20/100. Macula and Vision improved with Trusopt drops.
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 58355-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 58355-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 583
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Stargardt's Macular Dystrophy ABCA4 positivevaatamisi: 583 Fundus Autofluorescence shows central atrophy with Hyper FAF pisciform triradiate lesions. Images show some progression over 3 years of macular dystrophy.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CMEvaatamisi: 582CME worse - patient received subtenon's kenalog injection right eye.
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Stargardt's Macular Dystrophyvaatamisi: 58262 year old man with good vision
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26-year-old man choroideremia OU is 20/60vaatamisi: 58126-year-old man choroideremia OU is 20/60
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA Earlyvaatamisi: 58146-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Non-specific (uncharaterized / unknown) Macular Dystrophy vaatamisi: 58159-year-old man has macular dystrophy in both eyes. He had some vision changes in medical school in the 1980s and saw Dr. Gass for that. He had some pigment epithelial irregularities in both eyes. He had strabismus as a child and had muscle surgery. He is color blind, along with many people in his family, and as far as he knows, it is congenital.
20/25, 20/30
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 581
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Late Onset Retinal Degeneration (L-ORD)vaatamisi: 58155 year old with acute vision loss from a CNVM in the right eye. He responded to Lucentis therapy. His mother and her family has been confirmed genetically to have L-ORD and were part of the early reports.
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Stargardt's Macular Dystrophyvaatamisi: 58162 year old man with good vision
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Concentric Annular Macular Dystrophy 4/200 2/200 vision 61 Year Old Macular Crystalsvaatamisi: 58061-year-old woman has concentric annular macular dystrophy. She has had vision loss for 10 years who is no longer able to function even with the magnifiers and vision aids that she has. Her brother who is ten years younger than her, is recently diagnosed with the same macular dystrophy and her father and grandfather may have had similar problems in the past.
VISUAL ACUITY: OD 4/200, OS 2/200.
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Indocyanine Green Angiogram - Enhanced S Cone Syndrome - Goldmann Favre - vaatamisi: 58055-year-old woman while in college her vision was poor even with glasses and she sought evaluation for that. She was told after she had an electroretinogram at USF 15 years ago, that she had something with her blue cones. She does have poor night vision, but her reading vision is pretty good.
VISUAL ACUITY: OD 20/40, OS 20/40
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Stargardt's Macular Dystrophy ABCA4 positivevaatamisi: 579Images show some progression over 3 years of macular dystrophy.
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Pattern Dystrophy - Probably Early Butterflyvaatamisi: 57933 year old with normal vision and no visual complaints - normal color vision
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Best Disease for 30 Years - 20/50 Vision both eyes - 61 Year Old Womanvaatamisi: 57861-year-old woman was diagnosed with Best’s disease about 30 years ago. She and her many family members were tested, both at the VA Hospital and then at USF. OD 20/50, OS 20/50
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 57812-year-old had a dilated macular exam and the macula look abnormal. Interestingly, her mother, who is with her at this visit, was told about a year ago that her maculae are abnormal too. Her mother’s vision is fine. In the family tree, there are no known retinal dystrophies. They are both healthy.
VISUAL ACUITY: Her vision is 20/20 in both eyes.
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Fluorescein Angiogram - Enhanced S Cone Syndrome - Goldmann Favre - vaatamisi: 57855-year-old woman while in college her vision was poor even with glasses and she sought evaluation for that. She was told after she had an electroretinogram at USF 15 years ago, that she had something with her blue cones. She does have poor night vision, but her reading vision is pretty good.
VISUAL ACUITY: OD 20/40, OS 20/40
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Video - TAKES A LONG TIME TO LOAD - X-linked Juvenille Retinoschisis - Peripheral Retinal Vascular Anomalies - Vitreous Hemorrhage - 8 Year Old Boyvaatamisi: 5778-year-old child OD 20/40, OS 20/50
OD: Vertical C/D ratio is 0.2. There are foveal cysts. There is also a retinal elevation inferiorly and there are patchy peripheral retinal hemorrhages.
OS: Vertical C/D ratio is 0.2. There are foveal cysts. There is peripheral retinal issues with some hemorrhage in some areas of peripheral retinoschisis.
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Macular possible Cone Dystrophyvaatamisi: 577
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Choroideremia - Female Carrier - Patchy Atrophy of Choroid and RPE - Lyonizationvaatamisi: 576
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Late Onset Cone Dystrophy - Very Mildvaatamisi: 576Only IR and OCT show very mild bull's eye. 67 year old female with difficulty seeing in bright light
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Congenital Achromatopsia vaatamisi: 57526-year-old man was diagnosed with congenital achromatopsia by ERG as a child. He has family members who also have this disorder. OD 20/200, OS 20/200.
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X-linked Juvenille Retinoschisis - Peripheral Retinal Vascular Anomalies - Vitreous Hemorrhage - 8 Year Old Boyvaatamisi: 5758-year-old child OD 20/40, OS 20/50
OD: Vertical C/D ratio is 0.2. There are foveal cysts. There is also a retinal elevation inferiorly and there are patchy peripheral retinal hemorrhages.
OS: Vertical C/D ratio is 0.2. There are foveal cysts. There is peripheral retinal issues with some hemorrhage in some areas of peripheral retinoschisis.
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Retinitis Pigmentosa Sine Pigmento vaatamisi: 575
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 57455-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME- FA LATEvaatamisi: 57446-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Pattern Dystrophy - Probably Early Butterflyvaatamisi: 57333 year old with normal vision and no visual complaints - normal color vision
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Pattern Dystrophy - Probably Early Butterflyvaatamisi: 57333 year old with normal vision and no visual complaints - normal color vision
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Late Onset Cone Dystrophy - Very Mildvaatamisi: 572Only IR and OCT show very mild bull's eye. 67 year old female with difficulty seeing in bright light
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Stargardt's Disease - Macular Dystrophy - 69 Year Old African American Male - 20/200 both eyesvaatamisi: 57169-year-old man has had vision loss in both eyes starting 20 years ago. He was diagnosed at one point with Stargardt’s macular dystrophy. When I saw him, he had retinal atrophy in each eye.
Vision is 20/200 in each eye
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Retinitis Pigmentosa Sine Pigmento vaatamisi: 571
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 57055-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Alphamethlyacyl COA Racemase Deficiencyvaatamisi: 570
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA MIDvaatamisi: 57046-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Central Areolar Choroidal Dystrophyvaatamisi: 570Patient wanted second opinion for atrophic macular degeneration. VA is 20/400, right eye and 20/100. left eye. Patient has very poor vision and also hearing impaired. Fundiscopic exam reveals very atrophy in the macula. FAF shows a central hole to the choroid with no neovascularization present.
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Best Disease for 30 Years - 20/50 Vision both eyes - 61 Year Old Womanvaatamisi: 56961-year-old woman was diagnosed with Best’s disease about 30 years ago. She and her many family members were tested, both at the VA Hospital and then at USF. OD 20/50, OS 20/50
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Pigmented Peripheral Retinal Degenerationvaatamisi: 56942-year old male comes in for routine eye exam and to follow up on peripheral retinal degeneration in both eyes. VA is 20/20, right eye and 20/25, left eye. Patient is asymptomatic with no visual complaints.
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Stargardt's Macular Dystrophy ABCA4 positivevaatamisi: 569 Fundus Autofluorescence shows central atrophy with Hyper FAF pisciform triradiate lesions. Images show some progression over 3 years of macular dystrophy.
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 56855-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CME - FA MIDvaatamisi: 56846-year-old woman three of her 5 siblings have been diagnosed with retinitis pigmentosa. Her mother and father were seen and as far as everyone can tell, neither of them has it, although there was some thought they might be carriers. They were evaluated twenty five years ago and since then as far as she knows, there has not been a lot of testing done.
She has noticed a substantial decline in vision in both eyes over the last month or two. OD 20/40, OS 20/50. IOP: Both eyes have CME
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Late Onset Retinal Degeneration (L-ORD)vaatamisi: 56855 year old with acute vision loss from a CNVM in the right eye. He responded to Lucentis therapy. His mother and her family has been confirmed genetically to have L-ORD and were part of the early reports.
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Retinitis Pigmentosa Newly Diagnosed 55 Year Oldvaatamisi: 56755-year-old noticed his vision declining recently, over the last few weeks, particularly in the right eye. He said previous to that the vision was not normal but was pretty good. OD is 20/100, OS is 20/50
OCT SCAN: There is macular thickening in both eyes with intraretinal cysts.
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Retinitis Pigmentosa - Autosomal Dominant - Vision Loss at Young Age - Infraredvaatamisi: 567 54-year-old woman has autosomal dominant retinitis pigmentosa. Her mother and grandmother both had it and she has one son who has it and one daughter who doesn’t. She also has a sister with it. She lost vision since she was younger. She had cataract surgery done in January and February of this year. She has been seeing unusual flashing lights throughout the periphery and central vision for about the last year or two.
VISUAL ACUITY: OD 20/160, OS 20/160
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Non-specific (uncharaterized / unknown) Macular Dystrophy - FAFvaatamisi: 56759-year-old man has macular dystrophy in both eyes. He had some vision changes in medical school in the 1980s and saw Dr. Gass for that. He had some pigment epithelial irregularities in both eyes. He had strabismus as a child and had muscle surgery. He is color blind, along with many people in his family, and as far as he knows, it is congenital.
20/25, 20/30
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Late Onset Retinal Degeneration (L-ORD)vaatamisi: 56755 year old with acute vision loss from a CNVM in the right eye. He responded to Lucentis therapy. His mother and her family has been confirmed genetically to have L-ORD and were part of the early reports.
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Retinitis Pigmentosa - Autosomal Dominant - Vision Loss at Young Age - Infraredvaatamisi: 566 54-year-old woman has autosomal dominant retinitis pigmentosa. Her mother and grandmother both had it and she has one son who has it and one daughter who doesn’t. She also has a sister with it. She lost vision since she was younger. She had cataract surgery done in January and February of this year. She has been seeing unusual flashing lights throughout the periphery and central vision for about the last year or two.
VISUAL ACUITY: OD 20/160, OS 20/160
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Stargart's Macular Dystrophy Severevaatamisi: 56532-year-old man carries a diagnosis of Stargardt’s disease with poor vision in both eyes since he was 13. He has not noticed any substantial change since he was here 4 years ago.
VISUAL ACUITY: OD 10/200, OS 8/200
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Best Disease for 30 Years - 20/50 Vision both eyes - 61 Year Old Womanvaatamisi: 56561-year-old woman was diagnosed with Best’s disease about 30 years ago. She and her many family members were tested, both at the VA Hospital and then at USF. OD 20/50, OS 20/50
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Retinitis Pigmentosa Sine Pigmento or Unknown Dystrophy - Peripheral Superficial White Spots and Recurrent CMEvaatamisi: 5651 month of treatment with diamox 500 mg BID- cme is a little better
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Posterior Polar Annular Choroidal Dystrophyvaatamisi: 56568 year old woman with know macular irregularities for over 20 years. She has since been followed another 6 years and her vision remains 20/25.
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Non-specific (uncharaterized / unknown) Macular Dystrophy - FAFvaatamisi: 56559-year-old man has macular dystrophy in both eyes. He had some vision changes in medical school in the 1980s and saw Dr. Gass for that. He had some pigment epithelial irregularities in both eyes. He had strabismus as a child and had muscle surgery. He is color blind, along with many people in his family, and as far as he knows, it is congenital.
20/25, 20/30
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