Morphological and Functional Correlates in Goldmann-Favre Syndrome: A Case Series
Korean Journal of Ophthalmology
; : 143-146, 2012.
Article
in En
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| ID: wpr-40415
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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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Scotoma
/
Eye Diseases, Hereditary
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Macular Edema
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Retinoschisis
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Tomography, Optical Coherence
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Visual Field Tests
Limits:
Adult
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Humans
/
Male
Language:
En
Journal:
Korean Journal of Ophthalmology
Year:
2012
Type:
Article