Abstract
Purpose: We report a Korean case of concomitant keratoconus and granular corneal dystrophy type II. Methods: Case report. Results: A 29-year-old man visited our clinic for a routine ocular check-up. Slit-lamp examination revealed a few well-circumscribed, greyish-white, discrete granular opacities in the central corneal stromae of both eyes. Direct sequencing of exon 4 of the BIGH3 gene revealed a heterozygous transversion from G to A in the second-nucleotide position of codon 124. In addition, a Fleischer ring and Vogt's striae were evident in the cornea. The corneal topography was suggestive of keratoconus. Conclusion: Granular corneal dystrophy type II can co-exist with keratoconus and should be included in the differential diagnosis.
Original language | English |
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Pages (from-to) | 314-316 |
Number of pages | 3 |
Journal | Contact Lens and Anterior Eye |
Volume | 37 |
Issue number | 4 |
DOIs | |
State | Published - Aug 2014 |
Keywords
- BIGH3
- Corneal topography
- Granular corneal dystrophy
- Keratoconus