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Electroretinogrophic Finding of the Stargardt's Ddosease
Journal of the Korean Ophthalmological Society ; : 29-34, 1991.
Artículo en Coreano | WPRIM | ID: wpr-68725
ABSTRACT
Stargardt's disease is a heredo-macular dystrophy which evidences itself by reduced visual acuity, bilaterally, slowly progressive lesion, and by color blindness starting in youth. The diagnosis of Stargardt's disease is usually made by biomicroscopy and fluoresceine angiography which show many irregular shaped, small yellowish flecks. According to Fishman, the characteristic prolonged time to obtain adequate rod amplitude in dark-adapted electroretionography is advisable for differential diagnosis of Stargardt's disease. We didn't find the abnormal finding of dark-adapted electroretinography in two patients of Stargardt's disease. So, more studies will be needed for electroretinography of Stargardt's disease.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Angiografía / Agudeza Visual / Defectos de la Visión Cromática / Fluoresceína / Diagnóstico / Diagnóstico Diferencial / Electrorretinografía Tipo de estudio: Estudio diagnóstico Límite: Adolescente / Humanos Idioma: Coreano Revista: Journal of the Korean Ophthalmological Society Año: 1991 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Angiografía / Agudeza Visual / Defectos de la Visión Cromática / Fluoresceína / Diagnóstico / Diagnóstico Diferencial / Electrorretinografía Tipo de estudio: Estudio diagnóstico Límite: Adolescente / Humanos Idioma: Coreano Revista: Journal of the Korean Ophthalmological Society Año: 1991 Tipo del documento: Artículo