Skip to main content
Transactions of the American Ophthalmological Society logoLink to Transactions of the American Ophthalmological Society
. 1994;92:775–843.

A twin study on age-related macular degeneration.

S M Meyers
PMCID: PMC1298527  PMID: 7886884

Abstract

A prospective twin study on age-related macular degeneration (AMD) recruited 83 monozygotic pairs, 28 dizygotic pairs, and one triplet set from 1986 through 1993. Zygosity was determined by genetic testing of red cell markers, HLA antigens, or specific DNA loci. There were no twin pairs in which I collected data on only one twin. To decrease ascertainment bias, after 1991 the recruitment notice did not mention AMD, and I did not ask about a history of eye disease before the eye examination. Because of this, twin pairs recruited from 1986 through 1991 were statistically analyzed separately from those after January 1, 1992. From 1986 through 1991, 23 twin pairs were recruited; 11 monozygotic and 2 dizygotic pairs had nonAMD retinal changes or no retinal abnormalities, 9 monozygotic pairs with AMD were all concordant, and 1 dizygotic pair was discordant for basal laminar drusen. The concordance rate of AMD did not differ significantly between monozygotic and dizygotic twin pairs (P = .10) for 1986 through 1991. In 1992 and 1993, 88 twin pairs and one triplet set were recruited; 49 monozygotic and 19 dizygotic pairs had nonAMD retinal changes or no retinal abnormalities, 14 monozygotic pairs with AMD were all concordant, and 2 of 7 dizygotic pairs were concordant for AMD. The nonidentical triplets (1 with and 2 without AMD) were categorized as one of the discordant dizygotic pairs in the statistical evaluation. In nontwin age-matched (within 2 or 5 years of age) or age- and sex-matched sibling pairs the concordance rate of AMD ranged from 16% to 25%. The concordance rate of AMD was significantly higher in monozygotic than in dizygotic twins (P = .001) for 1992 and 1993. The concordance rate was higher for monozygotic twin pairs recruited in 1992 and 1993 than in any of the four subsets of nontwin age-method or age- and sex-matched sibling pairs (P < .0001). Overall, from 1986 through 1993, 23 of 23 monozygotic and 2 of 8 dizygotic twin pairs were concordant for AMD; this included the one dizygotic pair which was discordant for basal laminar drusen. The data of this study strongly suggest a genetic predisposition to AMD.

Full text

PDF
775

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abadi R. V., Dickinson C. M., Lomas M. S., Ackerley R. Congenital idiopathic nystagmus in identical twins. Br J Ophthalmol. 1983 Oct;67(10):693–695. doi: 10.1136/bjo.67.10.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bell J. A., Fielder A. R., Viney S. Congenital double elevator palsy in identical twins. J Clin Neuroophthalmol. 1990 Mar;10(1):32–34. [PubMed] [Google Scholar]
  3. Berson E. L., Rosner B., Sandberg M. A., Dryja T. P. Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His). Arch Ophthalmol. 1991 Jan;109(1):92–101. doi: 10.1001/archopht.1991.01080010094039. [DOI] [PubMed] [Google Scholar]
  4. Berson E. L., Rosner B., Sandberg M. A., Weigel-DiFranco C., Dryja T. P. Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine. Am J Ophthalmol. 1991 May 15;111(5):614–623. doi: 10.1016/s0002-9394(14)73708-0. [DOI] [PubMed] [Google Scholar]
  5. Blumenkranz M. S., Russell S. R., Robey M. G., Kott-Blumenkranz R., Penneys N. Risk factors in age-related maculopathy complicated by choroidal neovascularization. Ophthalmology. 1986 May;93(5):552–558. doi: 10.1016/s0161-6420(86)33702-3. [DOI] [PubMed] [Google Scholar]
  6. Bressler N. M., Bressler S. B., Seddon J. M., Gragoudas E. S., Jacobson L. P. Drusen characteristics in patients with exudative versus non-exudative age-related macular degeneration. Retina. 1988;8(2):109–114. doi: 10.1097/00006982-198808020-00005. [DOI] [PubMed] [Google Scholar]
  7. Bressler N. M., Bressler S. B., West S. K., Fine S. L., Taylor H. R. The grading and prevalence of macular degeneration in Chesapeake Bay watermen. Arch Ophthalmol. 1989 Jun;107(6):847–852. doi: 10.1001/archopht.1989.01070010869032. [DOI] [PubMed] [Google Scholar]
  8. Bucci F. A., Jr, Catalano R. A., Simon J. W. Discordance of accommodative esotropia in monozygotic twins. Am J Ophthalmol. 1989 Jan 15;107(1):84–85. doi: 10.1016/0002-9394(89)90822-2. [DOI] [PubMed] [Google Scholar]
  9. Castronuovo S., Simon J. W., Kandel G. L., Morier A., Wolf B., Witkop C. J., Jenkins P. L. Variable expression of albinism within a single kindred. Am J Ophthalmol. 1991 Apr 15;111(4):419–426. doi: 10.1016/s0002-9394(14)72374-8. [DOI] [PubMed] [Google Scholar]
  10. Chandra S. R., Gragoudas E. S., Friedman E., Van Buskirk E. M., Klein M. L. Natural history of disciform degeneration of the macula. Am J Ophthalmol. 1974 Oct;78(4):579–582. doi: 10.1016/s0002-9394(14)76293-2. [DOI] [PubMed] [Google Scholar]
  11. Cohen S. Y., Chretien P., Cochard C., Coscas G. J. Monozygotic twin sisters with adult vitelliform macular dystrophy. Am J Ophthalmol. 1993 Aug 15;116(2):246–247. doi: 10.1016/s0002-9394(14)71300-5. [DOI] [PubMed] [Google Scholar]
  12. Crawford M. J., Buckler J. M. Optic gliomata affecting twins with neurofibromatosis. Dev Med Child Neurol. 1983 Jun;25(3):370–373. doi: 10.1111/j.1469-8749.1983.tb13774.x. [DOI] [PubMed] [Google Scholar]
  13. Dryja T. P., McGee T. L., Hahn L. B., Cowley G. S., Olsson J. E., Reichel E., Sandberg M. A., Berson E. L. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa. N Engl J Med. 1990 Nov 8;323(19):1302–1307. doi: 10.1056/NEJM199011083231903. [DOI] [PubMed] [Google Scholar]
  14. Dryja T. P., McGee T. L., Reichel E., Hahn L. B., Cowley G. S., Yandell D. W., Sandberg M. A., Berson E. L. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature. 1990 Jan 25;343(6256):364–366. doi: 10.1038/343364a0. [DOI] [PubMed] [Google Scholar]
  15. Ebers G. C., Bulman D. E., Sadovnick A. D., Paty D. W., Warren S., Hader W., Murray T. J., Seland T. P., Duquette P., Grey T. A population-based study of multiple sclerosis in twins. N Engl J Med. 1986 Dec 25;315(26):1638–1642. doi: 10.1056/NEJM198612253152603. [DOI] [PubMed] [Google Scholar]
  16. Ferris F. L., 3rd, Fine S. L., Hyman L. Age-related macular degeneration and blindness due to neovascular maculopathy. Arch Ophthalmol. 1984 Nov;102(11):1640–1642. doi: 10.1001/archopht.1984.01040031330019. [DOI] [PubMed] [Google Scholar]
  17. Fishman G. A., Stone E. M., Gilbert L. D., Sheffield V. C. Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa. Arch Ophthalmol. 1992 May;110(5):646–653. doi: 10.1001/archopht.1992.01080170068026. [DOI] [PubMed] [Google Scholar]
  18. Fishman G. A., Stone E. M., Sheffield V. C., Gilbert L. D., Kimura A. E. Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa. Arch Ophthalmol. 1992 Jan;110(1):54–62. doi: 10.1001/archopht.1992.01080130056026. [DOI] [PubMed] [Google Scholar]
  19. Fishman G. A., Vandenburgh K., Stone E. M., Gilbert L. D., Alexander K. R., Sheffield V. C. Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa. Arch Ophthalmol. 1992 Nov;110(11):1582–1588. doi: 10.1001/archopht.1992.01080230082026. [DOI] [PubMed] [Google Scholar]
  20. Gass J. D. Drusen and disciform macular detachment and degeneration. Arch Ophthalmol. 1973 Sep;90(3):206–217. doi: 10.1001/archopht.1973.01000050208006. [DOI] [PubMed] [Google Scholar]
  21. Gregor Z., Bird A. C., Chisholm I. H. Senile disciform macular degeneration in the second eye. Br J Ophthalmol. 1977 Feb;61(2):141–147. doi: 10.1136/bjo.61.2.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Gregor Z., Joffe L. Senile macular changes in the black African. Br J Ophthalmol. 1978 Aug;62(8):547–550. doi: 10.1136/bjo.62.8.547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Gross L., Manfredi O. L., Protos A. A. Effect of cobalt-60 irradiation upon cell-mediated immunity. Radiology. 1973 Mar;106(3):653–655. doi: 10.1148/106.3.653. [DOI] [PubMed] [Google Scholar]
  24. Hamilton W. K., Ewing C. C., Ives E. J., Carruthers J. D. Sorsby's fundus dystrophy. Ophthalmology. 1989 Dec;96(12):1755–1762. doi: 10.1016/s0161-6420(89)32647-9. [DOI] [PubMed] [Google Scholar]
  25. Heckenlively J. R., Rodriguez J. A., Daiger S. P. Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin. Arch Ophthalmol. 1991 Jan;109(1):84–91. doi: 10.1001/archopht.1991.01080010086038. [DOI] [PubMed] [Google Scholar]
  26. Hofmann R. J. Monozygotic twins concordant for bilateral Duane's retraction syndrome. Am J Ophthalmol. 1985 May 15;99(5):563–566. doi: 10.1016/s0002-9394(14)77959-0. [DOI] [PubMed] [Google Scholar]
  27. Hrubec Z., Robinette C. D. The study of human twins in medical research. N Engl J Med. 1984 Feb 16;310(7):435–441. doi: 10.1056/NEJM198402163100706. [DOI] [PubMed] [Google Scholar]
  28. Hsieh R. C., Fine B. S., Lyons J. S. Patterned dystrophies of the retinal pigment epithelium. Arch Ophthalmol. 1977 Mar;95(3):429–435. doi: 10.1001/archopht.1977.04450030071006. [DOI] [PubMed] [Google Scholar]
  29. Hyman L. G., Lilienfeld A. M., Ferris F. L., 3rd, Fine S. L. Senile macular degeneration: a case-control study. Am J Epidemiol. 1983 Aug;118(2):213–227. doi: 10.1093/oxfordjournals.aje.a113629. [DOI] [PubMed] [Google Scholar]
  30. Johns D. R., Smith K. H., Miller N. R., Sulewski M. E., Bias W. B. Identical twins who are discordant for Leber's hereditary optic neuropathy. Arch Ophthalmol. 1993 Nov;111(11):1491–1494. doi: 10.1001/archopht.1993.01090110057023. [DOI] [PubMed] [Google Scholar]
  31. Kaiser-Kupfer M. I., Caruso R. C., Valle D. Gyrate atrophy of the choroid and retina. Long-term reduction of ornithine slows retinal degeneration. Arch Ophthalmol. 1991 Nov;109(11):1539–1548. doi: 10.1001/archopht.1991.01080110075039. [DOI] [PubMed] [Google Scholar]
  32. Kajiwara K., Sandberg M. A., Berson E. L., Dryja T. P. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens. Nat Genet. 1993 Mar;3(3):208–212. doi: 10.1038/ng0393-208. [DOI] [PubMed] [Google Scholar]
  33. Katz N. N., Whitmore P. V., Beauchamp G. R. Brown's syndrome in twins. J Pediatr Ophthalmol Strabismus. 1981 Jan-Feb;18(1):32–34. doi: 10.3928/0191-3913-19810101-09. [DOI] [PubMed] [Google Scholar]
  34. Kaufman L. W., Folk E. R., Miller M. T. Monozygotic twins discordant for Duane's retraction syndrome. Case report. Arch Ophthalmol. 1989 Mar;107(3):324–325. doi: 10.1001/archopht.1989.01070010334014. [DOI] [PubMed] [Google Scholar]
  35. Kim D. D., Mieler W. F., Wolf M. D. Posterior segment changes in membranoproliferative glomerulonephritis. Am J Ophthalmol. 1992 Nov 15;114(5):593–599. doi: 10.1016/s0002-9394(14)74489-7. [DOI] [PubMed] [Google Scholar]
  36. Kim R. Y., al-Maghtheh M., Fitzke F. W., Arden G. B., Jay M., Bhattacharya S. S., Bird A. C. Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5. Arch Ophthalmol. 1993 Nov;111(11):1518–1524. doi: 10.1001/archopht.1993.01090110084030. [DOI] [PubMed] [Google Scholar]
  37. Klein B. E., Klein R. Cataracts and macular degeneration in older Americans. Arch Ophthalmol. 1982 Apr;100(4):571–573. doi: 10.1001/archopht.1982.01030030573002. [DOI] [PubMed] [Google Scholar]
  38. Klein R., Davis M. D., Magli Y. L., Segal P., Klein B. E., Hubbard L. The Wisconsin age-related maculopathy grading system. Ophthalmology. 1991 Jul;98(7):1128–1134. doi: 10.1016/s0161-6420(91)32186-9. [DOI] [PubMed] [Google Scholar]
  39. Klein R., Klein B. E., Franke T. The relationship of cardiovascular disease and its risk factors to age-related maculopathy. The Beaver Dam Eye Study. Ophthalmology. 1993 Mar;100(3):406–414. doi: 10.1016/s0161-6420(93)31634-9. [DOI] [PubMed] [Google Scholar]
  40. Klein R., Klein B. E., Linton K. L. Prevalence of age-related maculopathy. The Beaver Dam Eye Study. Ophthalmology. 1992 Jun;99(6):933–943. doi: 10.1016/s0161-6420(92)31871-8. [DOI] [PubMed] [Google Scholar]
  41. Knobloch W. H., Leavenworth N. M., Bouchard T. J., Eckert E. D. Eye findings in twins reared apart. Ophthalmic Paediatr Genet. 1985 Feb;5(1-2):59–66. doi: 10.3109/13816818509007856. [DOI] [PubMed] [Google Scholar]
  42. Leibowitz H. M., Krueger D. E., Maunder L. R., Milton R. C., Kini M. M., Kahn H. A., Nickerson R. J., Pool J., Colton T. L., Ganley J. P. The Framingham Eye Study monograph: An ophthalmological and epidemiological study of cataract, glaucoma, diabetic retinopathy, macular degeneration, and visual acuity in a general population of 2631 adults, 1973-1975. Surv Ophthalmol. 1980 May-Jun;24(Suppl):335–610. [PubMed] [Google Scholar]
  43. Leslie R. D., Pyke D. A. Diabetic retinopathy in identical twins. Diabetes. 1982 Jan;31(1):19–21. doi: 10.2337/diab.31.1.19. [DOI] [PubMed] [Google Scholar]
  44. Marmor M. F., Byers B. Pattern dystrophy of the pigment epithelium. Am J Ophthalmol. 1977 Jul;84(1):32–44. doi: 10.1016/0002-9394(77)90320-8. [DOI] [PubMed] [Google Scholar]
  45. McWilliam P., Farrar G. J., Kenna P., Bradley D. G., Humphries M. M., Sharp E. M., McConnell D. J., Lawler M., Sheils D., Ryan C. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3. Genomics. 1989 Oct;5(3):619–622. doi: 10.1016/0888-7543(89)90031-1. [DOI] [PubMed] [Google Scholar]
  46. Melrose M. A., Magargal L. E., Lucier A. C. Identical twins with subretinal neovascularization complicating senile macular degeneration. Ophthalmic Surg. 1985 Oct;16(10):648–651. [PubMed] [Google Scholar]
  47. Meyers S. M., Zachary A. A. Monozygotic twins with age-related macular degeneration. Arch Ophthalmol. 1988 May;106(5):651–653. doi: 10.1001/archopht.1988.01060130705029. [DOI] [PubMed] [Google Scholar]
  48. Nichols B. E., Sheffield V. C., Vandenburgh K., Drack A. V., Kimura A. E., Stone E. M. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. Nat Genet. 1993 Mar;3(3):202–207. doi: 10.1038/ng0393-202. [DOI] [PubMed] [Google Scholar]
  49. Richards J. E., Kuo C. Y., Boehnke M., Sieving P. A. Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa. Ophthalmology. 1991 Dec;98(12):1797–1805. doi: 10.1016/s0161-6420(91)32047-5. [DOI] [PubMed] [Google Scholar]
  50. Rowland L. P., Hausmanowa-Petrusewicz I., Bardurska B., Warburton D., Nibroj-Dobosz I., DiMauro S., Pallai M., Johnson W. G. Kearns-Sayre syndrome in twins: lethal dominant mutation or acquired disease? Neurology. 1988 Sep;38(9):1399–1402. doi: 10.1212/wnl.38.9.1399. [DOI] [PubMed] [Google Scholar]
  51. SORSBY A., FRASER G. R. STATISTICAL NOTE ON THE COMPONENTS OF OCULAR REFRACTION IN TWINS. J Med Genet. 1964 Sep;1(1):47–49. doi: 10.1136/jmg.1.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Sarks J. P., Sarks S. H., Killingsworth M. C. Evolution of geographic atrophy of the retinal pigment epithelium. Eye (Lond) 1988;2(Pt 5):552–577. doi: 10.1038/eye.1988.106. [DOI] [PubMed] [Google Scholar]
  53. Sarks S. H. Ageing and degeneration in the macular region: a clinico-pathological study. Br J Ophthalmol. 1976 May;60(5):324–341. doi: 10.1136/bjo.60.5.324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Sarks S. H. Council Lecture. Drusen and their relationship to senile macular degeneration. Aust J Ophthalmol. 1980 May;8(2):117–130. doi: 10.1111/j.1442-9071.1980.tb01670.x. [DOI] [PubMed] [Google Scholar]
  55. Sarks S. H. Drusen patterns predisposing to geographic atrophy of the retinal pigment epithelium. Aust J Ophthalmol. 1982 May;10(2):91–97. doi: 10.1111/j.1442-9071.1982.tb00366.x. [DOI] [PubMed] [Google Scholar]
  56. Small K. W., Hermsen V., Gurney N., Fetkenhour C. L., Folk J. C. North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. One family, one disease. Arch Ophthalmol. 1992 Apr;110(4):515–518. doi: 10.1001/archopht.1992.01080160093040. [DOI] [PubMed] [Google Scholar]
  57. Sperduto R. D., Hiller R., Seigel D. Lens opacities and senile maculopathy. Arch Ophthalmol. 1981 Jun;99(6):1004–1008. doi: 10.1001/archopht.1981.03930011004003. [DOI] [PubMed] [Google Scholar]
  58. Spooner S. N., Bateman J. B., Yee R. D. Congenital nystagmus in identical twins: discordant features. J Pediatr Ophthalmol Strabismus. 1986 May-Jun;23(3):115–119. doi: 10.3928/0191-3913-19860501-04. [DOI] [PubMed] [Google Scholar]
  59. Stone E. M., Kimura A. E., Nichols B. E., Khadivi P., Fishman G. A., Sheffield V. C. Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene. Ophthalmology. 1991 Dec;98(12):1806–1813. doi: 10.1016/s0161-6420(91)32046-3. [DOI] [PubMed] [Google Scholar]
  60. Strahlman E. R., Fine S. L., Hillis A. The second eye of patients with senile macular degeneration. Arch Ophthalmol. 1983 Aug;101(8):1191–1193. doi: 10.1001/archopht.1983.01040020193003. [DOI] [PubMed] [Google Scholar]
  61. Taylor H. R., West S., Muñoz B., Rosenthal F. S., Bressler S. B., Bressler N. M. The long-term effects of visible light on the eye. Arch Ophthalmol. 1992 Jan;110(1):99–104. doi: 10.1001/archopht.1992.01080130101035. [DOI] [PubMed] [Google Scholar]
  62. Teikari J. M. Closed-angle glaucoma in 20 pairs of twins. Can J Ophthalmol. 1988 Feb;23(1):14–16. [PubMed] [Google Scholar]
  63. Teikari J. M. Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study. Acta Ophthalmol (Copenh) 1987 Dec;65(6):715–720. doi: 10.1111/j.1755-3768.1987.tb07069.x. [DOI] [PubMed] [Google Scholar]
  64. Teikari J. M., O'Donnell J. J. Astigmatism in 72 twin pairs. Cornea. 1989 Dec;8(4):263–266. [PubMed] [Google Scholar]
  65. Travis G. H., Hepler J. E. A medley of retinal dystrophies. Nat Genet. 1993 Mar;3(3):191–192. doi: 10.1038/ng0393-191. [DOI] [PubMed] [Google Scholar]
  66. Vaughn A. J., Bachman D., Sommer A. Neurofibromatosis in monozygotic twins: a case report of spontaneous mutation. Am J Med Genet. 1981;8(2):155–158. doi: 10.1002/ajmg.1320080205. [DOI] [PubMed] [Google Scholar]
  67. Weiter J. J., Delori F. C., Wing G. L., Fitch K. A. Relationship of senile macular degeneration to ocular pigmentation. Am J Ophthalmol. 1985 Feb 15;99(2):185–187. doi: 10.1016/0002-9394(85)90230-2. [DOI] [PubMed] [Google Scholar]
  68. Weleber R. G., Carr R. E., Murphey W. H., Sheffield V. C., Stone E. M. Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene. Arch Ophthalmol. 1993 Nov;111(11):1531–1542. doi: 10.1001/archopht.1993.01090110097033. [DOI] [PubMed] [Google Scholar]
  69. Wells J., Wroblewski J., Keen J., Inglehearn C., Jubb C., Eckstein A., Jay M., Arden G., Bhattacharya S., Fitzke F. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3(3):213–218. doi: 10.1038/ng0393-213. [DOI] [PubMed] [Google Scholar]
  70. Williams A., Eldridge R., McFarland H., Houff S., Krebs H., McFarlin D. Multiple sclerosis in twins. Neurology. 1980 Nov;30(11):1139–1147. doi: 10.1212/wnl.30.11.1139. [DOI] [PubMed] [Google Scholar]
  71. Wortham E., Crawford J. S. Brown's syndrome in twins. Am J Ophthalmol. 1988 May 15;105(5):562–563. doi: 10.1016/0002-9394(88)90257-7. [DOI] [PubMed] [Google Scholar]
  72. Zadnik K., Mannis M. J., Johnson C. A. An analysis of contrast sensitivity in identical twins with keratoconus. Cornea. 1984;3(2):99–103. [PubMed] [Google Scholar]
  73. de Jong P. T., Delleman J. W. Pigment epithelial pattern dystrophy. Four different manifestations in a family. Arch Ophthalmol. 1982 Sep;100(9):1416–1421. doi: 10.1001/archopht.1982.01030040394003. [DOI] [PubMed] [Google Scholar]

Articles from Transactions of the American Ophthalmological Society are provided here courtesy of American Ophthalmological Society

RESOURCES