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Retinose pigmentada unilateral secundária a trauma: relato de caso
(Conselho Brasileiro de Oftalmologia, 2012-06-01)
Retinitis pigmentosa is a group of diseases caused by genetic changes that lead to progressive degeneration of photoreceptors, rods mainly. In general, it has bilateral presentation. This study is a case report of a patient ...
Reabilitação visual em pacientes com retinose pigmentária
(Conselho Brasileiro de Oftalmologia, 2006-10-01)
PURPOSE: To determine which low-vision aids could be useful to patients with retinitis pigmentosa and also the benefits that the rehabilitation program could provide based on visual acuity and/or daily visual tasks. METHODS: ...
Pigmentary retinopathy due to Bardet-Biedl syndrome: case report and literature review
(Conselho Brasileiro de Oftalmologia, 2009-10-01)
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder with clinical and genetic heterogeneity. This syndrome was first described by Laurence and Moon in 1866 and additional cases were described by Bardet and ...
Acuidade visual e função de bastonetes em pacientes com retinose pigmentária
(Conselho Brasileiro de Oftalmologia, 2004-10-01)
PURPOSE: To investigate visual acuity and rod function, and correlate them to different clinical parameters in patients with retinitis pigmentosa (RP). METHODS: A cohort of 199 patients with retinitis pigmentosa (110 males ...
Análise multimodal em pacientes com Retinose Pigmentária relacionada ao gene EYS
(Universidade Federal de São Paulo, 2022)
Objetivo: A Retinose Pigmentária (RP) é uma doença que causa degeneração da retina, mais precisamente dos fotorreceptores, sendo de causa, principalmente, genética. Portanto, o objetivo deste trabalho foi compreender a ...
Classificação diagnóstica dos portadores de doenças degenerativas de retina, integrantes dos grupos Retina São Paulo e Retina Vale do Paraíba
(Conselho Brasileiro de Oftalmologia, 2003-08-01)
PURPOSE: To organize a regional data bank of all individuals that have retinal degenerative diseases, with the aim to classify each patient according to the type of distrophy and pattern of inheritance. METHODS: During the ...
Contribuição diagnóstica da avaliação eletrofisiológica visual em pacientes atendidos em hospital universitário
(Conselho Brasileiro de Oftalmologia, 2003-01-01)
PURPOSE: To determine the frequency of diagnostic categories obtained in a clinical vision electrophysiology laboratory at a university hospital. METHODS: Patients who underwent visual electrodiagnostic testing from October ...
Acuidade visual e eletrorretinografia de campo total em pacientes com síndrome de Usher
(Conselho Brasileiro de Oftalmologia, 2005-04-01)
PURPOSE: Usher's syndrome (US) is a group of genetically distinct autossomal conditions, characterized by sensorineural hearing loss accompanied by a retinal dystrophy indistinguishable from retinitis pigmentosa (RP). The ...