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Case Reports : Morphological and Functional Correlates in Goldmann-Favre Syndrome: A Case Series
( Madhavendra Bhandari ),( Rajni Rajan ),( P. Tandava Krishnan ),( Swakshyar Saumya Pal ),( Rajiv Raman ),( Tarun Sharma ) 대한안과학회 2012 Korean Journal of Ophthalmology Vol.26 No.2
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.