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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
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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
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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
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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
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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 ...
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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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The Heterogeneity of Leber's Congenital Amaurosis
Journal of Inherited Metabolic Disease, 1989Recent clinical and biochemical studies have revealed the existence of a ‘peroxisomal disorder’ originating in dysfunction of peroxisomes. In spite of intensive studies, the primary lesion of Zellweger syndrome is obscure (Aikawa et al., 1987). Johan et al. (1986) reported peroxisomal dysfunction in a boy with neurological symptoms and amaurosis.
J, Aikawa +4 more
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