
Morphological and Functional Correlates in Goldmann-Favre Syndrome: A Case Series
- Madhavendra Bhandari Rajni Rajan1, P. Tandava Krishnan Swakshyar Saumya Pal Rajiv Raman Tarun Sharma
- 대한안과학회
- The Korean Journal of Ophthalmology
- Vol.26 No.2
- 등재여부 : KCI등재
- 2012.04
- 143 - 146 (4 pages)
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.
Case Reports
Discussion
Conflict of Interest
References