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Morphological and Functional Correlates in Goldmann-Favre Syndrome: A Case Series
Korean J. Ophthalmol ; Korean J. Ophthalmol;: 143-146, 2012.
Article ي En | WPRIM | ID: wpr-40415
المكتبة المسؤولة: WPRO
ABSTRACT
The purpose of this study is to describe the correlation of findings between results from spectral domain optical coherence tomography (SD-OCT) and microperimetry in a case series regarding patients with Goldmann-Favre syndrome. Goldmann-Favre syndrome is a rare autosomal recessive hereditary vitreo-retinal degeneration that impacts the functionality of vision in subjects. Three men with this condition were assessed and subjected to microperimetry and SD-OCT. Two of the men were brothers. This study finds that the retinoschisis and macular cystoid changes noted in the SD-OCT matched the scotomas revealed by the microperimetry. The findings of each of the individual cases are reported herein.
الموضوعات
Key words
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Scotoma / Eye Diseases, Hereditary / Macular Edema / Retinoschisis / Tomography, Optical Coherence / Visual Field Tests المحددات: Adult / Humans / Male اللغة: En مجلة: Korean J. Ophthalmol السنة: 2012 نوع: Article
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Scotoma / Eye Diseases, Hereditary / Macular Edema / Retinoschisis / Tomography, Optical Coherence / Visual Field Tests المحددات: Adult / Humans / Male اللغة: En مجلة: Korean J. Ophthalmol السنة: 2012 نوع: Article