Kõrgeimalt hinnatud - Dystrophies
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Retinitis Pigmentosavaatamisi: 1659Patient comes in with cloudy vision. VA is 20/200 in both eyes. Patient has had retinal pigmentosa since 1986. Patient to consider cataract surgery to help her visual symptoms...
(2 hinnangut)
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Bullseye Maculopathy without Plaquinelvaatamisi: 1027Fundus photograph reveals Bull's-eye maculopathy without the use of plaquinel. Patients VA is 20/20, Right eye and 20/25, Left eye. There are reported cases of Scleroderma patients with retinal pigment epithelial atrophy. Will return for follow up in 6-months.
(2 hinnangut)
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Bullseye Maculopathy without Plaquinelvaatamisi: 1034Fundus photograph reveals Bull's-eye maculopathy without the use of plaquinel. Patients VA is 20/20, Right eye and 20/25, Left eye. There are reported cases of Scleroderma patients with retinal pigment epithelial atrophy. Will return for follow up in 6-months.
(2 hinnangut)
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Central Areolar Choroidal Dystrophyvaatamisi: 1271Patient 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.
(1 hinnangut)
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Cone Rod Dystrophyvaatamisi: 1060Cone Rod Dystrophy in OD of seven year old girl
(1 hinnangut)
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Retinal Pigmintosavaatamisi: 92128-year old female with no light perception in the right eye.
(1 hinnangut)
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Choroideremiavaatamisi: 116062-year old female who has extensive retinal damage in both eyes. VA 20/50 right eye, HM, left eye. Spot in vision, which is PSC, both eyes.
(1 hinnangut)
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Probable Measles Retinopathyvaatamisi: 126252-year old female wanted second opinion on retinal eval. Patient had PK and PDT in the left eye. VA was 20/30, right eye was count fingers. Pinhole was NI, both eyes. Patient's mother had measles. Notice pigment changes in both the color and FAF photo.
(1 hinnangut)
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Choroidal Dystrophyvaatamisi: 501
(1 hinnangut)
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Choroidal Dystrophyvaatamisi: 556
(1 hinnangut)
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Alphamethlyacyl COA Racemase Deficiencyvaatamisi: 1097
(1 hinnangut)
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Fundus Flavimaculatus - Stargardt Disease - 20/50 OD 20/200 OS 61 Year old Color Photovaatamisi: 167561-year-old decreasing vision for about the last five years. OD 20/50, OS 20/200.
Pisciform Lesions and Macular Atrophy
(1 hinnangut)
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Gyrate Atrophy - 15 year old male - 20/25 vision both eyes - Positive Family Historyvaatamisi: 81715 year old male was diagnosed with “retinitis pigmentosa†at age seven. The patient reports that his night vision is poor. He reports he does not notice a visual field change. He reports that his maternal grandfather has lost vision and a cousin has lost vision as well. He reports he has an uncle with some visual changes.
The most significantly affected relative is a 26-year-old legally blind cousin.
20/25+ OD, 20/25 OS.
(1 hinnangut)
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Pigmented Maculae - Mother and Daughter - Normal Visual Acuityvaatamisi: 63212-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.
(1 hinnangut)
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Stargardt's Juvenille Macular Dystrophy - Fundus Flavimaculatus - Famlialvaatamisi: 184055-year-old woman was seen in the office on 11/18/08. She has a half sister with Stargardt’s disease and seven other siblings who are fine. 20/120 OD, 20/160 OS.
(1 hinnangut)
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Stargart's Macular Dystrophy Severe - New Vitreomacular Asymptomatic Vitreomacular Traction ODvaatamisi: 67932-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
(1 hinnangut)
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Best Disease, Vitelliform Macular Dystrophy - 6 year old childvaatamisi: 878VISUAL ACUITY: Vision OD is 20/30, OS is 20/100.
(1 hinnangut)
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Malattia leventinesevaatamisi: 1961Basal laminar drusen in a perifoveal radial distribution are noted in this rare condition. Inheritance is AD with variable expressivity but full penetrance.
(7 hinnangut)
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Chorodial Sclerosisvaatamisi: 113374 year old female diagnosed with Chorodial Sclerosis OU and ARMD OU. Va 20/400 OD 2'200 OS
(3 hinnangut)
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Best Disease - Left Eye Treated Previously, Elsewhere, with PDT and Avastinvaatamisi: 120311-year-old has Best’s disease that runs in his family on his mothers side. At another retina specialists office, he had photodynamic laser in April of 2009 and Avastin subsequently in June of 2009. Unfortunately with that his vision is substantially declining. OD 20/30, OS 20/100
(2 hinnangut)
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Stargardt's Disease - Macular Dystrophy - 69 Year Old African American Male - 20/200 both eyesvaatamisi: 72669-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
(1 hinnangut)
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Cone-Rod Dystrophy vaatamisi: 146134-year-old woman who is having some difficulty seeing at night, especially navigating through dark movie theaters and dark restaurants. OD is 20/30, OS is 20/30
(1 hinnangut)
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Stargart's Macular Dystrophy Severevaatamisi: 68432-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
(1 hinnangut)
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Gyrate Atrophy - 15 year old male - 20/25 vision both eyes - Positive Family Historyvaatamisi: 94715 year old male was diagnosed with “retinitis pigmentosa†at age seven. The patient reports that his night vision is poor. He reports he does not notice a visual field change. He reports that his maternal grandfather has lost vision and a cousin has lost vision as well. He reports he has an uncle with some visual changes.
The most significantly affected relative is a 26-year-old legally blind cousin.
20/25+ OD, 20/25 OS.
(2 hinnangut)
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Indocyanine Green Angiogram - Enhanced S Cone Syndrome - Goldmann Favre - vaatamisi: 64255-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
(1 hinnangut)
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Stargardt's Disease - Macular Dystrophy - 69 Year Old African American Male - 20/200 both eyesvaatamisi: 92869-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
(1 hinnangut)
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Retinitis Pigmentosa - Leber's Congenital Amaurosis - 7 Year Old Child - Left Eyevaatamisi: 10817-year-old child who trips over things that the other children do not have trouble seeing. She is the only person in the family tree that the mother knows has any vision problems. Vision is 20/20 in each eye
(1 hinnangut)
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X-Linked Juvenille Retinoschisis 10 Year Old Child treated with Trusoptvaatamisi: 76210-year-old child has x-linked juvenile retinoschisis VA 20/60, OS is 20/100. Macula and Vision improved with Trusopt drops.
(1 hinnangut)
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