DAFTAR PUSTAKA

1. Ilyas, Sidharta. Ilmu Penyakit Mata. Edisi 3. Jakarta : Balai Penerbit FKUI : 2002. 2. Klintworth, dystrophies GK kornea. J Orphanet Langka Dis. 2009, 04:07 3. Szaflik JP, Oldak M, et al. Genetics of Meesmann corneal dystrophy. 2008, 27:S1-S42. 4. Meesmann A. Dominant Verterbte Dystrophia Epithelialis Corneae. Am J Hum Genet 1998, 63:1073-1077. 5. Klintworth GK, et al. : Identification of a new keratin K12 mutations associated with Stocker-Holt corneal dystrophy that differs from mutations found in Meesmann corneal dystrophy. Arch Ophthalmol 1955, 53:536. 6. Haddad R, et al. Unusual superficial variant of granular dystrophy of the cornea. Klin Monatsbl Augenheilkd 1949, 114:386-397. 7. Wittebol-Post D, Pels E. The dystrophy described by Reis and Bucklers. Separate entity or variant of the granular dystrophy?. Ophthalmology 1983, 90:1507-1511 8. Klintworth GK, et al. Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin gene. Arch Ophthalmol 1980, 98:144-148. 9. Ren Z, et al. Mutations of the M1S1 gene on chromosome 1P in autosomal recessive gelatinous drop-like corneal dystrophy. Mol Vis 1998, 4:31. 10. Lisch W, et al. A new, band-shaped and whorled microcystic dystrophy of the corneal epithelium. Proc Internat Soc Eye Res 2000, 71:S108P. 11. Lisch W, et al. Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to Xp22.3. Am J Ophthalmol 1992, 114:35-44. 12. Hammar B, et al. A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance. Am J Ophthalmol 1994, 117:543-544. 13. Wales HJ. A family history of corneal erosions. Acta Ophthalmol (Copenh) 1967, 45:829-836. 14. Klintworth GK, et al : Macular corneal dystrophy. Lack of keratan sulfate in serum and cornea. Arch Ophthalmol 1993, 111:1106-1114.

15. Klintworth GK, et al. CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review. Mol Vis 2000, 6:261-264. 16. Klintworth GK, et al. Accumulation of ig-h3 gene product in corneas with granular dystrophy. Acta Ophthalmol (Copenh) 1990, 68:384-389. 17. Munier FL, et al. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. Am J Hum Genet 1998, 62:320-324. 18. Akimune C, et al. Corneal guttata associated with the corneal dystrophy resulting from a betaig-h3 R124H mutation. Mol Vis 2007, 13:1390-1396 19. Holland EJ, et al. Avellino corneal dystrophy. Clinical manifestations and natural history. Cornea 1999, 18:424-429 20. Weiss JS. Visual morbidity in thirty-four families with Schnyder crystalline corneal dystrophy. Jpn J Ophthalmol 1998, 42:450-455. 21. Purcell JJ Jr, et al. Fleck corneal dystrophy. Am J Ophthalmol 1977, 83:55460 22. Vithana EN, et al. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Arch Ophthalmol 1978, 96:2036-2039. 23. Biswas S, et al. Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Orphanet J Rare Dis 2008, 3:28. 24. Harissi-Dagher M, et al. Keratoglobus in association with posterior polymorphous dystrophy. Albrecht von Graefes Arch Klin Exp Ophthalmol 1916, 91:363-379. 25. Toma NMG,et al. Linkage of congenital hereditary endothelial dystrophy to chromosome 20. Cornea 2000, 19:570-573 26. Schmid E,et al. A new, X-linked endothelial corneal dystrophy. Klin Monatsbl Augenheilkd 1976, 169:717-727 27. Rumah Sakit Mata Dr. Yap
singapura national eye centre. http://www.snec.com.sg/about/international/menuutama/pelayananklinis/subspecialties/Corneal-and-External-EyeDisease/corneal-surgery-clinical-services/Pages/Cornea_Transplantation.aspx