Erratum: IC3D Classification of Corneal Dystrophies-Edition 2 (Cornea DOI: 10.1097/ICO.0000000000000307);IC3D classification of corneal dystrophies-edition 2

Cornea

Volumn 34, Issue 2, 2015, Pages 117-159

  Weiss, Jayne S ^a   Møller, Hans Ulrik ^b   Aldave, Anthony J ^c   Seitz, Berthold ^d   Bredrup, Cecilie ^e   Kivelä, Tero ^f   Munier, Francis L ^g   Rapuano, Christopher J ^h   Nischal, Kanwal K ⁱ   Kim, Eung Kweon ^j   Sutphin, John ^k   Busin, Massimo ^l   Labbé, Antoine ^m   Kenyon, Kenneth R ⁿ   Kinoshita, Shigeru ^o   Lisch, Walter ^p  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b AARHUS UNIVERSITY HOSPITAL   (Denmark)

^c JULES STEIN EYE INSTITUTE   (United States)

^d SAARLAND UNIVERSITY   (Germany)

^e HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^f UNIVERSITY OF HELSINKI   (Finland)

^g JULES GONIN EYE HOSPITAL   (Switzerland)

^h WILLS EYE HOSPITAL   (United States)

ⁱ UNIVERSITY OF PITTSBURGH   (United States)

^j Yonsei University   (South Korea)

^k UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

^l Villa Igea Hospital   (Italy)

^m CENTRE HOSPITALIER NATIONAL D OPHTALMOLOGIE DES QUINZE VINGTS   (France)

ⁿ TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^o KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^p UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

more..

Author keywords

Bowman membrane; Centralcloudy dystrophy of Fran ois; Confocal microscopy; Congenital corneal endothelial dystrophy and X linked endothelialdystrophy; Congenital stromal corneal dystrophy; Cornea; Cornea dystrophy; Cornea pathology; Descemetmembrane; Endothelial dystrophies; Endothelium; Epithelial and subepithelial dystrophies; Epithelial basement membranedystrophy; Epithelial recurrent erosion dystrophies; Epithelial stromal TGFBI dystrophies; Epithelium; Fleck corneal dystrophy; Fuchsendothelial corneal dystrophy; Gelatinousdrop like corneal dystrophy; Genetic disease; Genetics; Granular corneal dystrophy type 1; Granular corneal dystrophy type 2; Hereditary disease; Histology; Histopathology; Keratoconus; Lattice corneal dystrophy; Lisch epithelial corneal dystrophy; Macular corneal dystrophy; Meesmann dystrophy; Posterior amorphous corneal dystrophy; Posteror polymorphous corneal dystrophy; Pre Descemet corneal dystrophy; Reis B cklers corneal dystrophy; Schnyder corneal dystrophy; Stroma; Stromal dystrophies; Subepithelialmucinous corneal dystrophy; TGFBI; Thiel Behnke corneal dystrophy

Indexed keywords

2008 INTERNATIONAL CLASSIFICATION OF CORNEA DYSTROPHY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME; CHROMOSOME 20; CONFOCAL MICROSCOPY; CONGENITAL CORNEA DYSTROPHY; CORNEA DYSTROPHY; DISEASE CLASSIFICATION; EPITHELIAL AND SUBEPITHELIAL DYSTROPHY; EPITHELIAL STROMAL TGFBI DYSTROPHY; EROSION; EYE PHOTOGRAPHY; FRANCESCHETTI CORNEAL DYSTROPHY; GENE LOCUS; GENETIC ASSOCIATION; HISTOPATHOLOGY; HUMAN; INHERITANCE; KERATOCONUS; MEDICAL TERMINOLOGY; PEER REVIEW; PRIORITY JOURNAL; RECURRENT DISEASE; STROMAL DYSTROPHY; THIEL BEHNKE CORNEAL DYSTROPHY; TRANSMISSION ELECTRON MICROSCOPY; CLASSIFICATION; GENETICS; INTERNATIONAL CLASSIFICATION OF DISEASES; NOMENCLATURE; PATHOLOGY;

CORNEAL DYSTROPHIES, HEREDITARY; HUMANS; INTERNATIONAL CLASSIFICATION OF DISEASES; TERMINOLOGY AS TOPIC;

EID: 84925829555     PISSN: 02773740     EISSN: 15364798     Source Type: Journal    
DOI: 10.1097/ICO.0000000000003175     Document Type: Erratum

References (46)

1. Weiss JS, Møller HU, Lisch W, et al. The IC3D classification of the corneal dystrophies [in English and Spanish]. Cornea. 2008;27(suppl 2):S1-S83.
2. Groenouw A. Knoetchenfoermige Hornhauttruebungen (Noduli corneae). Arch Augenheilkd. 1890;21:281-289.
3. Biber H. Ueber einige seltene Hornhauterkrankungen: die oberflaechliche gittrige Keratitis [Inaugural Dissertation]. A Diggelmann Zuerich. 1890.
4. Fuchs E. Dystrophia epithelialis corneae. Arch Ophthalmol. 1910;76:478-508.
5. Uthoff W. Ein Fall von doppelseitiger zentraler, punktfoermiger, supepithelialer knoetchenfoermiger Keratitis, Groenouw mit anatomischem Befunde. Klin Monatsbl Augenheilkd. 1915;54:377-383.
6. Yoshida Y. Ueber eine neue Art der Dystrophia corneae mit histologischem Befunde. Albrecht von Graefes Arch Clin Exp Ophthalmol. 1924;114:91-100.
7. Afshari NA, Bouchard CS, Colby KA, de Freitas D, Rootman DS, Tu EY, Weisenthal RW. Corneal dystrophies and ectasias. In: Weisenthal RW, ed. 2014-2015 Basic and Clinical Science Course, Section 8: External Disease and Cornea. San Francisco; American Academy of Ophthalmology; 2014:253-287.
8. Aldave AJ, Yellore VS, Salem AK, et al. No VSX1 gene mutations associated with keratoconus. Invest Ophthalmol Vis Sci. 2006;47:2820-2822.
9. Dash DP, George S, O'Prey D, et al. Mutational screening of VSX1 in keratoconus patients from the European population. Eye (Lond). 2010;24:1085-1092.
10. Edwards M, McGhee CN, Dean S. The genetics of keratoconus. Clin Experiment Ophthalmol. 2001;29:345-351.
11. Rabinowitz YS. The genetics of keratoconus. Ophthalmol Clin North Am. 2003;16:607-620.
12. Tyynismaa H, Sistonen P, Tuupanen S, et al. A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. Invest Ophthalmol Vis Sci. 2002;43:3160-3164.
13. Wang Y, Rabinowitz YS, Rotter JI, et al. Genetic epidemiological study of keratoconus: evidence for major gene determination. Am J Med Genet. 2000;93:403-409.
14. Waring GO III, Rodrigues MM, Laibson PR. Corneal dystrophies. I. Dystrophies of the epithelium, Bowman's layer and stroma. Surv Ophthalmol. 1978;23:71-122.
15. Waring GO III, Rodrigues MM, Laibson PR. Corneal dystrophies. II. Endothelial dystrophies. Surv Ophthalmol. 1978;23:147-168.
16. François J. Une nouvelle dystrophie hérédo-familiale de la cornée. J Genet Hum. 1956;5:189-196.
17. Strachan IM. Cloudy central corneal dystrophy of François. Five cases in the same family. Br J Ophthalmol. 1969;53:192-194.
18. Bramsen T, Ehlers N, Baggesen LH. Central cloudy corneal dystrophy of François. Acta Ophthalmol (Copenh). 1976;54:221-226.
19. Karp CL, Scott IU, Green WR, et al. Central cloudy corneal dystrophy of François. A clinicopathologic study. Arch Ophthalmol. 1997;115:1058-1062.
20. Krachmer JH, Purcell JJ Jr, Young CW, et al. Corneal endothelial dystrophy. A study of 64 families. Arch Ophthalmol. 1978;96:2036-2039.
21. Hamill CE, Schmedt T, Jurkunas U. Fuchs endothelial cornea dystrophy: a review of the genetics behind disease development. Semin Ophthalmol. 2013;28:281-286.
22. Weiss JS. Schnyder's dystrophy of the cornea. A Swede-Finn connection. Cornea. 1992;11:93-101.
23. Weiss JS. Schnyder crystalline dystrophy sine crystals. Recommendation for a revision of nomenclature. Ophthalmology. 1996;103:465-473.
24. Weiss JS. Visual morbidity in 34 families with Schnyder's crystalline corneal dystrophy. A clinical pathologic report with quantitative analysis of corneal lipid composition. Ophthalmology. 1994;101:895-901.
25. Aldave AJ, Edward DP, Park AJ, et al. Central discoid corneal dystrophy. Cornea. 2002;21:739-744.
26. Weiss JS, Wiaux C, Yellore V, et al. Reported p. Asp240Asn mutation in UBIAD1 suggests central discoid corneal dystrophy is a variant of Schnyder corneal dystrophy. Cornea. 2010;29:777-780.
27. Orr A, Dubé MP, Marcadier J, et al. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy. PLoS One. 2007;2:e685.
28. Weiss JS, Kruth HS, Kuivaniemi H, et al. Mutations in the UBIAD1 gene on chromosome short arm 1, region 36 cause Schnyder crystalline corneal dystrophy. Invest Ophthalmol Vis Sci. 2007;48:5007-5012.
29. Grayson M, Wilbrandt H. Dystrophy of the anterior limiting membrane of the cornea (Reis-Bueckler type). Am J Ophthalmol. 1966;61:345-349.
30. Bouchard CS, Coroneo MT, Florakis GJ, et al. Corneal dystrophies and ectasias. In: Reidy JJ, ed. 2010-2011 Basic and Clinical Science Course, Section 8: External Disease and Cornea. San Francisco, CA: American Academy of Ophthalmology; 2010:267-303.
31. Kanai A, Waltman S, Polack FM, et al. Electron microscopic study of hereditary corneal edema. Invest Ophthalmol. 1971;10:89-99.
32. Kanai A, Kaufman HE. Further electron microscopy study of hereditary corneal edema. Invest Ophthalmol. 1971;10:545-554.
33. Levenson JE, Chandler JW, Kaufman HE. Affected asymptomatic relatives in congenital hereditary endothelial dystrophy. Am J Ophthalmol. 1973;76:967-971.
34. Aldave AJ, Han J, Frausto RF. Genetics of the corneal endothelial dystrophies: an evidence-based review. Clin Genet. 2013;84:109-119.
35. Yee RW, Sullivan LS, Lai HT, et al. Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24. Genomics. 1997;46:152-154.
36. Lohse E, Stock LE, Jones JC, et al. Reis-Büecklers' corneal dystrophy. Immunofluorescent and electron microscopic studies. Cornea. 1989;8:200-209.
37. Nakamura H, Li FT, Folterman MO, et al. Individual phenotypic variances in a family with Thiel-Behnke corneal dystrophy. Cornea. 2012;31:1217-1222.
38. Lisch W, Kivelä T. Individual phenotypic variances in a family with Thiel-Behnke corneal dystrophy. Cornea. 2013;32:e192-e193.
39. Franceschetti A. Hereditaere rezidivierende Erosion der Hornhaut. Z Augenheilk. 1928;66:309-316.
40. Hammar B, Bjöerck E, Lagerstedt K, et al. A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance. Acta Ophthalmol. 2008;86:758-763.
41. Lisch W, Bron AJ, Munier FL, et al. Franceschetti hereditary recurrent corneal erosion. Am J Ophthalmol. 2012;153:1073-1081.e4.
42. Hammar B, Bjöerck E, Lind H, et al. Dystrophia Helsinglandica: a new type of hereditary corneal recurrent erosions with late subepithelial fibrosis. Acta Ophthalmol. 2009;87:659-665.
43. Møller HU. "Corneal dystrophies". In: Hoyt C, Taylor D, eds. Paediatric Ophthalmology and Strabismus. 4th ed. Elsevier Science; 2012:323-328.
44. Hu M, Kestelyn P, Weiss JS. Pediatric corneal dystrophies. A plea for pictures. Cornea. 2010;29:1469.
45. Lisch W, Saikia P, Pitz S, et al. Chameleon-like appearance of immunotactoid keratopathy. Cornea. 2012;31:55-58.
46. ®: a novel approach to combine clinical testing and researching genetic ocular disease. Curr Opin Ophthalmol. 2012;23:355-363.