Optic Atrophy Diagnosis
Mostrando 1-12 de 13 artigos, teses e dissertações.
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1. Síndrome de Wolfram - Diagnóstico clínico de condição rara multissistêmica
Resumo A Síndrome de Wolfram consiste em uma patologia neurodegenerativa de caráter genético, também conhecida pela sigla DIDMOAD que traduz os principais achados dessa doença, Diabetes Insipidus, Diabetes Mellitus, Atrofia Óptica e Surdez. O artigo visa relatar ocaso de um paciente diagnosticado clinicamente com essa síndrome em um ambulatório geral
Rev. bras.oftalmol.. Publicado em: 02/12/2019
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2. Correlação entre parâmetros cardiovasculares e alterações glaucomatosas do nervo óptico em portadores de insuficiência cardíaca congestiva
Resumo Objetivos: Correlacionar parâmetros oftalmoscópicos e cardiovasculares em pacientes com diagnóstico de insuficiência cardíaca com fração de ejeção reduzida (ICFER) e avaliar a associação entre ICFER e alterações do nervo óptico sugestivas de glaucoma. Métodos: Estudo descritivo, observacional, prospectivo, composto por amostra 30 paci
Rev. bras.oftalmol.. Publicado em: 13/05/2019
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3. Caracterização motora e funcional da paraplegia espástica, atrofia óptica e neuropatia periférica (síndrome Spoan) / Functional and motor characterization of spastic paraplegia, optic atrophy and peripheral neuropathy
INTRODUCTION: Spoan syndrome is a complex form of spastic paraplegia of recessive inheritance recently identified in individuals from Southwest of Rio Grande do Norte state. Clinical features are characterized by congenital optic atrophy, progressive spastic paraplegia, and axonal neuropathy, resulting in severe handicap. Phenotypic description of this disea
Publicado em: 2009
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4. "Análise comparativa das medidas de espessura da camada de fibras nervosas da retina de pacientes com atrofia em banda do nervo óptico e de indivíduos normais através da tomografia de coerência óptica e da polarimetria a laser" / A comparative analysis of the retinal nerve fiber layer thickness measurements in patients with band atrophy of the optic nerve and in normal controls using optical coherence tomography and scanning laser polarimetry
Most diseases that affect the optic pathways present clinically with loss of one or more visual functions.When optic pathway injuries involve the anterior visual pathways they may cause loss of the retinal nerve fiber layer (RNFL) and "band atrophy" (BA). The purpose of this study was therefore to compare the ability of the optical coherence tomography (OCT)
Publicado em: 2006
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5. Wolfram (DIDMOAD) syndrome.
Wolfram syndrome (MIM 222300) is the association of juvenile onset diabetes mellitus and optic atrophy, also known as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness). Patients present with diabetes mellitus followed by optic atrophy in the first decade, cranial diabetes insipidus and sensorineural deafness in the second decade, d
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6. Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.
A syndrome is described, consisting of severe neurogenic distal wasting, generalised muscle weakness, absent ankle reflexes, pyramidal signs, mental retardation, optic atrophy and retinal colloid bodies. A sural nerve biopsy from one case showed loss of nerve fibres suggesting the diagnosis of hereditary motor and sensory neuropathy. Progression of the disor
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7. The Alström syndrome: ophthalmic histopathology and retinal ultrastructure.
A case of pigmentary retinal degeneration causing blindness in early childhood, progressive neurosensory hearing loss, diabetes mellitus, acanthosis nigricans, hypogonadism with normal secondary sex characteristics, and kyphoscoliosis without polydactyly and with no mental retardation is reported. The results of endocrinological studies, karyotype analysis,
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8. Reappraisal of the ratio of disc to macula/disc diameter in optic nerve hypoplasia.
The ratio of disc to macula/disc diameter is characteristically increased in eyes with optic nerve hypoplasia. We present the largest reported series of patients with a definitive diagnosis of optic nerve hypoplasia for whom this ratio has been determined. All measurements were made by an independent masked observer. Our results are in accordance with previo
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9. Acute presumed histoplasmosis of the optic nerve head.
A 38-year-old man from the Ohio Valley area presented to the Ophthalmology Cinic at a west coast hospital (USA) because of sudden loss of the right inferior temporal visual field after severe right frontal headache of several hours' duration. During the following months, diffuse peripapillary atrophy and peripheral punched-out lesions developed. When he had
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10. Eye signs in craniopharyngioma.
A total of 45 patients with craniopharyngioma are reviewed, with particular reference to the presenting clinical features and neuro-ophthalmological findings. Of these 50 per cent had been referred in the first instance to an eye clinic. More than half the children presented with the clinical picture of raised intracranial pressure, although one-third of the
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11. Late ocular manifestations in neonatal herpes simplex infection.
Five patients who had had neonatal herpes simplex virus infection were re-examined at ages that varied from 6 to 9 years. In all of them the diagnosis had been supported by virus isolation and antibody titration, and herpes virus type 2, the genital strain, had been the causative agent. Only 1 of the patients was mentally retarded. Three of the patients had
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12. Ophthalmology in Luanda (Angola): a hospital based report.
AIMS/BACKGROUND--As part of a 4 year Spanish development aid programme, an ophthalmic hospital was set up in Luanda in 1991 for the in situ training of local ophthalmologists. Presented here are the data obtained from 4201 patients treated during the first 2 years of the project. METHODS--Patients were referred to the institute from the emergency ward at the