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Morphological and functional correlates in Goldmann-Favre syndrome: a case series
Madhavendra Bhandari1, Rajni Rajan, P Tandava Krishnan
1Elite School of Optometry, Sankara Nethralaya, Chennai, Tamil Nadu, India. madhavendra_opto@yahoo.co.in
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.
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