Results 171 to 180 of about 18,407 (215)
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Survey of Ophthalmology, 1997
A 36-year-old healthy woman developed amaurosis fugax of the right eye lasting 1 minute. Work-up revealed right carotid stenosis thought most compatible with an atherosclerotic plaque. A carotid endarterectomy was performed which corroborated the radiologic diagnosis.
Michael L Slavin, M L Slavin
exaly +3 more sources
A 36-year-old healthy woman developed amaurosis fugax of the right eye lasting 1 minute. Work-up revealed right carotid stenosis thought most compatible with an atherosclerotic plaque. A carotid endarterectomy was performed which corroborated the radiologic diagnosis.
Michael L Slavin, M L Slavin
exaly +3 more sources
Amaurosis Fugax: Is it Innocuous?
Annals of Vascular Surgery, 1992A 10 year retrospective study of 103 patients with amaurosis fugax was done. Sixty-two patients with symptoms of amaurosis fugax underwent arteriography, which demonstrated ulcerated carotid plaque in 36 and hemodynamically significant stenoses (greater than 75% diameter reduction) in 26. These 62 patients underwent carotid endarterectomy. The other 41
D, Rosenthal +5 more
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American Journal of Ophthalmology, 1978
A 57-year-old alcoholic man sustained permanent bilateral blindness and optic atrophy as a complication of hemorrhage from peptic ulcer disease. Post-hemorrhagic visual loss occurs in middle-aged, debilitated persons a short time after repeated episodes of hemorrhage from any site.
K M, Klewin, R E, Appen, P L, Kaufman
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A 57-year-old alcoholic man sustained permanent bilateral blindness and optic atrophy as a complication of hemorrhage from peptic ulcer disease. Post-hemorrhagic visual loss occurs in middle-aged, debilitated persons a short time after repeated episodes of hemorrhage from any site.
K M, Klewin, R E, Appen, P L, Kaufman
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Molecular Genetics and Metabolism, 1999
Leber's congenital amaurosis (LCA) is the earliest and most severe form of all inherited retinal dystrophies responsible for congenital blindness. Genetic heterogeneity of LCA has been suspected since the report by Waardenburg of normal children born to affected parents.
I, Perrault +9 more
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Leber's congenital amaurosis (LCA) is the earliest and most severe form of all inherited retinal dystrophies responsible for congenital blindness. Genetic heterogeneity of LCA has been suspected since the report by Waardenburg of normal children born to affected parents.
I, Perrault +9 more
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La Revue du praticien, 1995
Amaurosis is an organic loss of visual acuity which can attain blindness and which occurs suddenly in the absence of other ophthalmological changes. It constitutes an ophthalmologic emergency requiring a careful aetiologic work-up in order to determine therapy. We will discuss various aetiologies of amaurosis and its treatment.
M, Schaison-Cusin, C, Vignal-Clermont
openaire +1 more source
Amaurosis is an organic loss of visual acuity which can attain blindness and which occurs suddenly in the absence of other ophthalmological changes. It constitutes an ophthalmologic emergency requiring a careful aetiologic work-up in order to determine therapy. We will discuss various aetiologies of amaurosis and its treatment.
M, Schaison-Cusin, C, Vignal-Clermont
openaire +1 more source
2018
Leber congenital amaurosis (LCA) is a part of the spectrum of early-onset retinal dystrophy (EORD). It usually presents in the first few years of life, most often before the age of 1 year. The prevalence is about 1:80,000. Also known as congenital retinitis pigmentosa (RP), patients have wandering nystagmus, with reduced vision from birth.
Stephen H, Tsang, Tarun, Sharma
openaire +3 more sources
Leber congenital amaurosis (LCA) is a part of the spectrum of early-onset retinal dystrophy (EORD). It usually presents in the first few years of life, most often before the age of 1 year. The prevalence is about 1:80,000. Also known as congenital retinitis pigmentosa (RP), patients have wandering nystagmus, with reduced vision from birth.
Stephen H, Tsang, Tarun, Sharma
openaire +3 more sources
American Journal of Ophthalmology, 1966
In two families with congenital amaurosis of Leber, keratoglobus was found in all affected members and posterior subcapsular cataracts in most of them. Consanguinity was present in one family. Pathologic findings in one enucleated eye were presented. The literature on this disease was briefly reviewed.
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In two families with congenital amaurosis of Leber, keratoglobus was found in all affected members and posterior subcapsular cataracts in most of them. Consanguinity was present in one family. Pathologic findings in one enucleated eye were presented. The literature on this disease was briefly reviewed.
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Acta Ophthalmologica, 1983
Forty‐four unselected patients with amaurosis fugax (AF) have been followed for 4.6 years (mean 2.6). Thirty per cent had atheromatous lesions, 20% had miscellaneous diagnoses (temporal arteritis 5, transitory ocular hypertension 2, glaucomatous iritis 1, benign intracraniel hypertension 1), 50% consisted of young, mainly women, in whom no cause was ...
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Forty‐four unselected patients with amaurosis fugax (AF) have been followed for 4.6 years (mean 2.6). Thirty per cent had atheromatous lesions, 20% had miscellaneous diagnoses (temporal arteritis 5, transitory ocular hypertension 2, glaucomatous iritis 1, benign intracraniel hypertension 1), 50% consisted of young, mainly women, in whom no cause was ...
openaire +2 more sources