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A 48-year-old man presents with bilateral corneal deposits
Digital Journal of Ophthalmology 2009
Volume 15, Number 4
November 27, 2009
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Shaminder S. Bhullar, MD | Krieger Eye Institute, Sinai Hospital
Gerami D. Seitzman, MD | Krieger Eye Institute, Sinai Hospital
References
1. Mannis MJ. The stromal dystrophies. In: Krachmer et al. Eds. Cornea, USA: St. Louis, 1997; chap. 89.
2. Korvatska E, Munier FL, Djemaï A., et al. Mutation hot spots in 5q31-linked corneal dystrophies. Am J Hum Genet 1998;62(2):320-4.
3. Hilton EN, Black GC, Manson FD, et al. De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy. Br J Ophthalmol 2007;91(8):1083-4.
4. Kim JW, Kim HM, Song JS. Phenotypic non-penetrance in granular corneal dystrophy type II. Graefes Arch Clin Exp Ophthalmol 2008;246(11):1629-31.
5. Meallet MA, Affeldt JA, McFarland TJ, et al. An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His beta iG-H3 mutation in an African-American woman. Am J Ophthalmol 2004;137(4);765-7.
6. Salouti R, Hosseini H, Eghtedari M, Khalili MR. Deep anterior lamellar keratoplasty with Melles technique for granular corneal dystrophy. Cornea 2009;28(2):140-3.
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