Optic Atrophy Diagnostic
Mostrando 1-7 de 7 artigos, teses e dissertações.
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1. Correlação entre as espessuras da mácula e da camada de fibras nervosas da retina, medidas pelas tomografias de coerência óptica de dominio Fourier e de domínio do tempo, e a perimetria automatizada na atrofia em banda do nervo óptico / Correlation between macular and retinal nerve fiber layer Fourier domain and time domain optical coherence tomography measurements and visual field loss in band atrophy of the optic nerve
PURPOSE: To investigate the relationship between fourier-domain optical coherence tomography (FD - OCT) measured macular and retinal nerve fiber layer thickness (RNFL) and visual field sensitivity loss on standard automated perimetry in eyes with permanent temporal hemianopia from chiasmal compression and compare the ability of FD - OCT and time-domain optic
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 18/04/2011
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2. Correlação entre o eletrorretinograma de padrão reverso, a tomografia de coerência óptica e a perimetria automatizada na detecção da perda neural na atrofia em banda do nervo óptico / Relationship between pattern electroretinogram, optical coherence tomography and automated perimetry for detection of neural loss in eyes with band atrophy of the optic nerve
PURPOSE: To evaluate the ability of full-field and hemifield pattern electroretinogram parameters to differentiate between healthy eyes and eyes with band atrophy of the optic nerve and also to evaluate the relationship between pattern electroretinogram amplitude, macular and retinal nerve fiber layer thickness by optical coherence tomography, and visual fie
Publicado em: 2010
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3. Comparação das medidas da espessura macular e da camada de fibras nervosas retiniana para detecção de atrofia em banda do nervo óptico através da tomografia de coerência óptica / Comparison of macular thickness and retinal nerve fiber thickness measurements for detection of band atrophy of the optic nerve using optical coherence tomography
Pacientes com compressão quiasmática apresentam perda das fibras nervosas da retina nasal que decussam no quiasma óptico. Por conseguinte, ocorre perda das fibras nervosas, predominantemente, no setor nasal e temporal do disco óptico, que se manifesta por atrofia em banda do nervo óptico ao exame oftalmoscópico e hemianopsia temporal ao exame de campo
Publicado em: 2007
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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. Diagnostic criteria and genetics of the PEHO syndrome.
The PEHO syndrome (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy) is a recently recognised disorder of unknown biochemical background. Diagnostic features have been found in neuroradiological and neuropathological studies, which show characteristic severe cerebellar atrophy. In combined neuroradiological and ophthalmological studi
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7. 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