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Editorial

Fuchs’ endothelial corneal dystrophy: fostering change in clinical care using observational data

, &
Pages 389-391 | Published online: 09 Jan 2014

References

  • Musch DC, Niziol LM, Stein JD, Kamyar RM, Sugar A. Prevalence of corneal dystrophies in the United States: estimates from claims data. Invest. Ophthalmol. Vis. Sci. 52(9), 6959–6963 (2011).
  • Eye Bank Association of America. 2011 Eye Banking Statistical Report. Eye Bank Association of America, Washington, DC, USA (2011).
  • Price MO, Gorovoy M, Benetz BA et al. Descemet’s stripping automated endothelial keratoplasty outcomes compared with penetrating keratoplasty from the Cornea Donor Study. Ophthalmology 117(3), 438–444 (2010).
  • Price MO, Fairchild KM, Price DA, Price FW Jr. Descemet’s stripping endothelial keratoplasty five-year graft survival and endothelial cell loss. Ophthalmology 118(4), 725–729 (2011).
  • Dapena I, Ham L, Droutsas K, van Dijk K, Moutsouris K, Melles GR. Learning curve in Descemet’s membrane endothelial keratoplasty: first series of 135 consecutive cases. Ophthalmology 118(11), 2147–2154 (2011).
  • Guerra FP, Anshu A, Price MO, Giebel AW, Price FW. Descemet’s membrane endothelial keratoplasty: prospective study of 1-year visual outcomes, graft survival, and endothelial cell loss. Ophthalmology 118(12), 2368–2373 (2011).
  • Kopplin LJ, Przepyszny K, Schmotzer B et al.; Fuchs’ Endothelial Corneal Dystrophy Genetics Multi-Center Study Group. Relationship of Fuchs’ endothelial corneal dystrophy severity to central corneal thickness. Arch. Ophthalmol. 130(4), 433–439 (2012).
  • Pitts JF, Jay JL. The association of Fuchs’ corneal endothelial dystrophy with axial hypermetropia, shallow anterior chamber, and angle closure glaucoma. Br. J. Ophthalmol. 74(10), 601–604 (1990).
  • Nagarsheth M, Singh A, Schmotzer B et al.; for the Fuchs’ Genetics Multi-Center Study Group. Relationship between Fuchs’ endothelial corneal dystrophy severity and glaucoma and/or ocular hypertension. Arch. Ophthalmol. doi:10.1001/archophthalmol.2012.1969 (2012) (Epub ahead of print).
  • Loutitt MD, Kopplin LJ, Igo RP Jr et al. A multi-center study to map genes for Fuchs’ endothelial corneal dystrophy: baseline characteristics and heritability. Cornea 31(1), 26–35 (2012).
  • Zhang X, Fondran J, Igo RP Jr, Oliva M, Lass JH, Iyengar SK. The relationship of smoking and other risk factors to severity of Fuchs’ endothelial corneal dystrophy. Presented at: Association for Research in Vision and Ophthalmology Annual Meeting. Fort Lauderdale, FL, USA, 6–10 May 2012.
  • Krachmer JH, Purcell JJ Jr, Young CW, Bucher KD. Corneal endothelial dystrophy. A study of 64 families. Arch. Ophthalmol. 96(11), 2036–2039 (1978).
  • Biswas S, Munier FL, Yardley J et al. Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum. Mol. Genet. 10(21), 2415–2423 (2001).
  • Gottsch JD, Sundin OH, Liu SH et al. Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of Fuchs’ corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 46(6), 1934–1939 (2005).
  • Baratz KH, Tosakulwong N, Ryu E et al. E2-2 protein and Fuchs’ corneal dystrophy. N. Engl. J. Med. 363(11), 1016–1024 (2010).
  • Igo RP, Kopplin LJ, Joseph P et al. Differing roles for TCF4 and COL8A2 in central corneal thickness and Fuchs’ endothelial corneal dystrophy. PLoS ONE 7(10), e46742 (2012)
  • Jun AS, Meng H, Ramanan N et al. An alpha 2 collagen VIII transgenic knock-in mouse model of Fuchs’ endothelial corneal dystrophy shows early endothelial cell unfolded protein response and apoptosis. Hum. Mol. Genet. 21(2), 384–393 (2012).
  • Mackey DA, Warrington NM, Hewitt AW et al. Role of the TCF4 gene intronic variant in normal variation of corneal endothelium. Cornea 31(2), 162–166 (2012).
  • Brunette I, Sherknies D, Terry MA, Chagnon M, Bourges JL, Meunier J. 3-D characterization of the corneal shape in Fuchs’ dystrophy and pseudophakic keratopathy. Invest. Ophthalmol. Vis. Sci. 52(1), 206–214 (2011).
  • Meadows DN, Eghrari AO, Riazuddin SA, Emmert DG, Katsanis N, Gottsch JD. Progression of Fuchs’ corneal dystrophy in a family linked to the FCD1 locus. Invest. Ophthalmol. Vis. Sci. 50(12), 5662–5666 (2009).

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