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. 1995 Jul;79(7):697–702. doi: 10.1136/bjo.79.7.697

X linked retinoschisis.

N D George 1, J R Yates 1, A T Moore 1
PMCID: PMC505202  PMID: 7662639

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  1. Alexander K. R., Fishman G. A. Rod-cone interaction in flicker perimetry: evidence for a distal retinal locus. Doc Ophthalmol. 1985 Aug 15;60(1):3–36. doi: 10.1007/BF00164567. [DOI] [PubMed] [Google Scholar]
  2. Alitalo T., Forsius H., Kärnä J., Frants R. R., Eriksson A. W., Wood S., Kruse T. A., de la Chapelle A. Linkage relationships and gene order around the locus for X-linked retinoschisis. Am J Hum Genet. 1988 Oct;43(4):476–483. [PMC free article] [PubMed] [Google Scholar]
  3. Alitalo T., Kruse T. A., Ahrens P., Albertsen H. M., Eriksson A. W., de la Chapelle A. Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region. Hum Genet. 1991 Apr;86(6):599–603. doi: 10.1007/BF00201548. [DOI] [PubMed] [Google Scholar]
  4. Alitalo T., Kruse T. A., de la Chapelle A. Refined localization of the gene causing X-linked juvenile retinoschisis. Genomics. 1991 Mar;9(3):505–510. doi: 10.1016/0888-7543(91)90417-d. [DOI] [PubMed] [Google Scholar]
  5. Anderson J. R. ANTERIOR DIALYSIS OF THE RETINA: DISINSERTION OR AVULSION AT THE ORA SERRATA. Br J Ophthalmol. 1932 Dec;16(12):641–670. doi: 10.1136/bjo.16.12.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Arden G. B., Gorin M. B., Polkinghorne P. J., Jay M., Bird A. C. Detection of the carrier state of X-linked retinoschisis. Am J Ophthalmol. 1988 Jun 15;105(6):590–595. doi: 10.1016/0002-9394(88)90049-9. [DOI] [PubMed] [Google Scholar]
  7. Arden G. B., Hogg C. R. Rod-cone interactions and analysis of retinal disease. Br J Ophthalmol. 1985 Jun;69(6):404–415. doi: 10.1136/bjo.69.6.404. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Arkfeld D. F., Brockhurst R. J. Vascularized vitreous membranes in congenital retinoschisis. Retina. 1987 Spring;7(1):20–23. [PubMed] [Google Scholar]
  9. BALIAN J. V., FALLS H. F. Congenital vascular veils in the vitreous; hereditary retinoschisis. Arch Ophthalmol. 1960 Jan;63:92–101. doi: 10.1001/archopht.1960.00950020094014. [DOI] [PubMed] [Google Scholar]
  10. BARUT C. Périphlébite rétinienne associée à des lésions maculaires constatée chez deux frères et évoluant depuis l'enfance. Bull Soc Ophtalmol Fr. 1955 Mar;3:185–188. [PubMed] [Google Scholar]
  11. Barnstable C. J. A molecular view of vertebrate retinal development. Mol Neurobiol. 1987 Spring-Summer;1(1-2):9–46. doi: 10.1007/BF02935263. [DOI] [PubMed] [Google Scholar]
  12. Basmadjian G., Labelle P., Dumas J. The natural evolution of juvenile retinoschisis (presentation of a case). Can J Ophthalmol. 1973 Jan;8(1):33–37. [PubMed] [Google Scholar]
  13. Bengtsson B., Linder B. Sex-linked hereditary juvenile retinoschisis: presentation of two affected families. Acta Ophthalmol (Copenh) 1967;45(3):411–423. doi: 10.1111/j.1755-3768.1967.tb06506.x. [DOI] [PubMed] [Google Scholar]
  14. Biancalana V., Briard M. L., David A., Gilgenkrantz S., Kaplan J., Mathieu M., Piussan C., Poncin J., Schinzel A., Oudet C. Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. Am J Hum Genet. 1992 May;50(5):981–987. [PMC free article] [PubMed] [Google Scholar]
  15. Biancalana V., Trivier E., Weber C., Weissenbach J., Rowe P. S., O'Riordan J. L., Partington M. W., Heyberger S., Oudet C., Hanauer A. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene. Genomics. 1994 Aug;22(3):617–625. doi: 10.1006/geno.1994.1435. [DOI] [PubMed] [Google Scholar]
  16. Brockhurst R. J. Photocoagulation in congenital retinoschisis. Arch Ophthalmol. 1970 Aug;84(2):158–165. doi: 10.1001/archopht.1970.00990040160007. [DOI] [PubMed] [Google Scholar]
  17. Brodrick J. D., Wyatt H. T. Hereditary sex-linked retinoschisis. Br J Ophthalmol. 1973 Aug;57(8):551–559. doi: 10.1136/bjo.57.8.551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Condon G. P., Brownstein S., Wang N. S., Kearns J. A., Ewing C. C. Congenital hereditary (juvenile X-linked) retinoschisis. Histopathologic and ultrastructural findings in three eyes. Arch Ophthalmol. 1986 Apr;104(4):576–583. doi: 10.1001/archopht.1986.01050160132029. [DOI] [PubMed] [Google Scholar]
  19. Constantaras A. A., Dobbie J. G., Choromokos E. A., Frenkel M. Juvenile sex-linked recessive retinoschisis in a black family. Am J Ophthalmol. 1972 Dec;74(6):1166–1178. doi: 10.1016/0002-9394(72)90739-8. [DOI] [PubMed] [Google Scholar]
  20. Conway B. P., Welch R. B. X-chromosone-linked juvenile retinoschisis with hemorrhagic retinal cyst. Am J Ophthalmol. 1977 Jun;83(6):853–855. doi: 10.1016/0002-9394(77)90913-8. [DOI] [PubMed] [Google Scholar]
  21. Dahl N., Goonewardena P., Chotai J., Anvret M., Pettersson U. DNA linkage analysis of X-linked retinoschisis. Hum Genet. 1988 Mar;78(3):228–232. doi: 10.1007/BF00291666. [DOI] [PubMed] [Google Scholar]
  22. De Becker I., Riddell D. C., Dooley J. M., Tremblay F. Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype. Br J Ophthalmol. 1994 Sep;78(9):719–722. doi: 10.1136/bjo.78.9.719. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ewing C. C., Cullen A. P. Fluorescein angiography in X-chromosomal maculopathy with retinoschisis (juvenile hereditary retinoschisis). Can J Ophthalmol. 1972 Jan;7(1):19–28. [PubMed] [Google Scholar]
  24. Ewing C. C., Ives E. J. Juvenile hereditary retinoschisis. Trans Ophthalmol Soc U K. 1970;89:29–39. [PubMed] [Google Scholar]
  25. Fishman G. A., Jampol L. M., Goldberg M. F. Diagnostic features of the Favre-Goldmann syndrome. Br J Ophthalmol. 1976 May;60(5):345–353. doi: 10.1136/bjo.60.5.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Foos R. Y. Vitreoretinal juncture; topographical variations. Invest Ophthalmol. 1972 Oct;11(10):801–808. [PubMed] [Google Scholar]
  27. Forsius H., Krause U., Helve J., Vuopala V., Mustonen E., Vainio-Mattila B., Fellman J., Eriksson A. W. Visual acuity in 183 cases of X-chromosomal retinoschisis. Can J Ophthalmol. 1973 Jul;8(3):385–393. [PubMed] [Google Scholar]
  28. Forsius H., Vainio-Mattila B., Eriksson A. X-LINKED HEREDITARY RETINOSCHISIS. Br J Ophthalmol. 1962 Nov;46(11):678–681. doi: 10.1136/bjo.46.11.678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. GIESER E. P., FALLS H. F. Hereditary retinoschisis. Am J Ophthalmol. 1961 Jun;51:1193–1200. doi: 10.1016/0002-9394(61)92457-6. [DOI] [PubMed] [Google Scholar]
  30. GOODMAN G., RIPPS H., SIEGEL I. M. SEX-LINKED OCULAR DISORDERS: TRAIT EXPRESSIVITY IN MALES AND CARRIER FEMALES. Arch Ophthalmol. 1965 Mar;73:387–398. doi: 10.1001/archopht.1965.00970030389018. [DOI] [PubMed] [Google Scholar]
  31. George N. D., Yates J. R., Bradshaw K., Moore A. T. Infantile presentation of X linked retinoschisis. Br J Ophthalmol. 1995 Jul;79(7):653–657. doi: 10.1136/bjo.79.7.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Goldberg S. H., Frumkes T. E., Nygaard R. W. Inhibitory influence of unstimulated rods in the human retina: evidence provided by examining cone flicker. Science. 1983 Jul 8;221(4606):180–182. doi: 10.1126/science.6857279. [DOI] [PubMed] [Google Scholar]
  33. Green J. L., Jr, Jampol L. M. Vascular opacification and leakage in X-linked (juvenile) retinoschisis. Br J Ophthalmol. 1979 May;63(5):368–373. doi: 10.1136/bjo.63.5.368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Greven C. M., Moreno R. J., Tasman W. Unusual manifestations of X-linked retinoschisis. Trans Am Ophthalmol Soc. 1990;88:211–228. [PMC free article] [PubMed] [Google Scholar]
  35. Harris G. S., Yeung J. Maculopathy of sex-linked juvenile retinoschisis. Can J Ophthalmol. 1976 Jan;11(1):1–10. [PubMed] [Google Scholar]
  36. Hung J. Y., Hilton G. F. Neovascular glaucoma in a patient with X-linked juvenile retinoschisis. Ann Ophthalmol. 1980 Sep;12(9):1054–1055. [PubMed] [Google Scholar]
  37. Ide C. H., Wilson R. J. Juvenile retinoschisis. Br J Ophthalmol. 1973 Aug;57(8):560–562. doi: 10.1136/bjo.57.8.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Karowski C. J., Proenza L. M. Relationship between Müller cell responses, a local transretinal potential, and potassium flux. J Neurophysiol. 1977 Mar;40(2):244–259. doi: 10.1152/jn.1977.40.2.244. [DOI] [PubMed] [Google Scholar]
  39. Kawano K., Tanaka K., Murakami F., Ohba N. Congenital hereditary retinoschisis: evolution at the initial stage. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1981;217(4):315–323. doi: 10.1007/BF00429292. [DOI] [PubMed] [Google Scholar]
  40. Kellner U., Brümmer S., Foerster M. H., Wessing A. X-linked congenital retinoschisis. Graefes Arch Clin Exp Ophthalmol. 1990;228(5):432–437. doi: 10.1007/BF00927256. [DOI] [PubMed] [Google Scholar]
  41. Kellner U., Foerster M. H. Cone dystrophies with negative photopic electroretinogram. Br J Ophthalmol. 1993 Jul;77(7):404–409. doi: 10.1136/bjo.77.7.404. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. LEVY J. Inherited retinal detachment. Br J Ophthalmol. 1952 Nov;36(11):626–636. doi: 10.1136/bjo.36.11.626. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. LYON M. F. Sex chromatin and gene action in the mammalian X-chromosome. Am J Hum Genet. 1962 Jun;14:135–148. [PMC free article] [PubMed] [Google Scholar]
  44. Laatikainen L., Tarkkanen A., Saksela T. Hereditary X-linked retinoschisis and bilateral congenital retinal detachment. Retina. 1987 Spring;7(1):24–27. [PubMed] [Google Scholar]
  45. Lewis R. A., Lee G. B., Martonyi C. L., Barnett J. M., Falls H. F. Familial foveal retinoschisis. Arch Ophthalmol. 1977 Jul;95(7):1190–1196. doi: 10.1001/archopht.1977.04450070088006. [DOI] [PubMed] [Google Scholar]
  46. Mann I., Macrae A. CONGENITAL VASCULAR VEILS IN THE VITREOUS. Br J Ophthalmol. 1938 Jan;22(1):1–10. doi: 10.1136/bjo.22.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Manschot W. A. Pathology of hereditary conditions related to retinal detachment. Ophthalmologica. 1971;162(4):223–234. doi: 10.1159/000306280. [DOI] [PubMed] [Google Scholar]
  48. Manschot W. A. Pathology of hereditary juvenile retinoschisis. Arch Ophthalmol. 1972 Aug;88(2):131–138. doi: 10.1001/archopht.1972.01000030133002. [DOI] [PubMed] [Google Scholar]
  49. Miller R. F., Dowling J. E. Intracellular responses of the Müller (glial) cells of mudpuppy retina: their relation to b-wave of the electroretinogram. J Neurophysiol. 1970 May;33(3):323–341. doi: 10.1152/jn.1970.33.3.323. [DOI] [PubMed] [Google Scholar]
  50. Miyake Y., Miyake S., Yanagida K., Kanda T. [X-chromosomal congenital retinoschisis--its fundus polymorphism and visual function (author's transl)]. Nippon Ganka Gakkai Zasshi. 1981 Feb;85(2):97–112. [PubMed] [Google Scholar]
  51. Miyake Y., Shiroyama N., Ota I., Horiguchi M. Focal macular electroretinogram in X-linked congenital retinoschisis. Invest Ophthalmol Vis Sci. 1993 Mar;34(3):512–515. [PubMed] [Google Scholar]
  52. Miyake Y., Yagasaki K., Horiguchi M., Kawase Y., Kanda T. Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol. 1986 Jul;104(7):1013–1020. doi: 10.1001/archopht.1986.01050190071042. [DOI] [PubMed] [Google Scholar]
  53. Nasr Y. G., Cherfan G. M., Michels R. G., Wilkinson C. P. Goldmann-Favre maculopathy. Retina. 1990;10(3):178–180. [PubMed] [Google Scholar]
  54. Newman E. A. Regional specialization of retinal glial cell membrane. Nature. 1984 May 10;309(5964):155–157. doi: 10.1038/309155a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Newton M. S., Collyer S., Phillips C. I. Male proband with X linked retinoschisis apparently inherited from his father's family. J Med Genet. 1991 Mar;28(3):213–214. doi: 10.1136/jmg.28.3.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Noble K. G., Carr R. E., Siegel I. M. Familial foveal retinoschisis associated with a rod-cone dystrophy. Am J Ophthalmol. 1978 Apr;85(4):551–557. doi: 10.1016/s0002-9394(14)75254-7. [DOI] [PubMed] [Google Scholar]
  57. Peachey N. S., Fishman G. A., Derlacki D. J., Brigell M. G. Psychophysical and electroretinographic findings in X-linked juvenile retinoschisis. Arch Ophthalmol. 1987 Apr;105(4):513–516. doi: 10.1001/archopht.1987.01060040083038. [DOI] [PubMed] [Google Scholar]
  58. Pearson R., Jagger J. Sex linked juvenile retinoschisis with optic disc and peripheral retinal neovascularisation. Br J Ophthalmol. 1989 Apr;73(4):311–313. doi: 10.1136/bjo.73.4.311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Peralta S., Santori M. Degenerazione maculare centrale tipo Stargardt associata ad alterazioni vitreali congenite. Ann Ottalmol Clin Ocul. 1967 Mar;93(3):237–242. [PubMed] [Google Scholar]
  60. Pillers D. A., Bulman D. E., Weleber R. G., Sigesmund D. A., Musarella M. A., Powell B. R., Murphey W. H., Westall C., Panton C., Becker L. E. Dystrophin expression in the human retina is required for normal function as defined by electroretinography. Nat Genet. 1993 May;4(1):82–86. doi: 10.1038/ng0593-82. [DOI] [PubMed] [Google Scholar]
  61. Regillo C. D., Tasman W. S., Brown G. C. Surgical management of complications associated with X-linked retinoschisis. Arch Ophthalmol. 1993 Aug;111(8):1080–1086. doi: 10.1001/archopht.1993.01090080076021. [DOI] [PubMed] [Google Scholar]
  62. Reichenbach A., Stolzenburg J. U., Eberhardt W., Chao T. I., Dettmer D., Hertz L. What do retinal müller (glial) cells do for their neuronal 'small siblings'? J Chem Neuroanat. 1993 Jul-Aug;6(4):201–213. doi: 10.1016/0891-0618(93)90042-3. [DOI] [PubMed] [Google Scholar]
  63. Reichenbach A., Ziegert M., Schnitzer J., Pritz-Hohmeier S., Schaaf P., Schober W., Schneider H. Development of the rabbit retina. V. The question of 'columnar units'. Brain Res Dev Brain Res. 1994 May 13;79(1):72–84. doi: 10.1016/0165-3806(94)90050-7. [DOI] [PubMed] [Google Scholar]
  64. Rowe P. S., Goulding J., Read A., Lehrach H., Francis F., Hanauer A., Oudet C., Biancalana V., Kooh S. W., Davies K. E. Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2). Hum Genet. 1994 Mar;93(3):291–294. doi: 10.1007/BF00212025. [DOI] [PubMed] [Google Scholar]
  65. Rowe P. S., Goulding J., Read A., Mountford R., Hanauer A., Oudet C., Whyte M. P., Meier-Ewert S., Lehrach H., Davies K. E. New markers for linkage analysis of X-linked hypophosphataemic rickets. Hum Genet. 1993 Jul;91(6):571–575. doi: 10.1007/BF00205082. [DOI] [PubMed] [Google Scholar]
  66. Rudanko S. L., Flage T., Hansen E., Rosenberg T., Viggosson G., Riise R. Visual impairment in Nordic children. V. X-linked juvenile retinoschisis. Acta Ophthalmol (Copenh) 1993 Oct;71(5):586–589. doi: 10.1111/j.1755-3768.1993.tb04646.x. [DOI] [PubMed] [Google Scholar]
  67. SORSBY A., KLEIN M., GANN J. H., SIGGINS G. Unusual retinal detachment possibly sex-linked. Br J Ophthalmol. 1951 Jan;35(1):1–10. doi: 10.1136/bjo.35.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Sabates F. N. Juvenile retinoschisis. Am J Ophthalmol. 1966 Oct;62(4):683–688. doi: 10.1016/0002-9394(66)92194-5. [DOI] [PubMed] [Google Scholar]
  69. Schepens C. L. Congenital retinoschisis. Klin Oczna. 1988 Apr-May;90(4-5):127–132. [PubMed] [Google Scholar]
  70. Schulman J., Peyman G. A., Jednock N., Larson B. Indications for vitrectomy in congenital retinoschisis. Br J Ophthalmol. 1985 Jul;69(7):482–486. doi: 10.1136/bjo.69.7.482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Sieving P. A., Bingham E. L., Roth M. S., Young M. R., Boehnke M., Kuo C. Y., Ginsburg D. Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes. Am J Hum Genet. 1990 Oct;47(4):616–621. [PMC free article] [PubMed] [Google Scholar]
  72. Tanino T., Katsumi O., Hirose T. Electrophysiological similarities between two eyes with X-linked recessive retinoschisis. Doc Ophthalmol. 1985 Aug 30;60(2):149–161. doi: 10.1007/BF00158030. [DOI] [PubMed] [Google Scholar]
  73. Tasman W., Greven C., Moreno R. Nasal retinal dragging in X-linked retinoschisis. Graefes Arch Clin Exp Ophthalmol. 1991;229(4):319–322. doi: 10.1007/BF00170688. [DOI] [PubMed] [Google Scholar]
  74. Thomson E. MEMORANDUM: Regarding a Family in which Neuro-Retinal Disease of an unusual kind occurred only in the Males. Br J Ophthalmol. 1932 Dec;16(12):681–686. doi: 10.1136/bjo.16.12.681. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Turut P., François P., Castier P., Milazzo S. Analysis of results in the treatment of peripheral retinoschisis in sex-linked congenital retinoschisis. Graefes Arch Clin Exp Ophthalmol. 1989;227(4):328–331. doi: 10.1007/BF02169406. [DOI] [PubMed] [Google Scholar]
  76. Vainio-Mattila B., Eriksson A. W., Forsius H. X-chromosomal recessive retinoschisis in the Region of Pori. An ophthalmo-genetical analysis of 103 cases. Acta Ophthalmol (Copenh) 1969;47(5):1135–1148. doi: 10.1111/j.1755-3768.1969.tb02513.x. [DOI] [PubMed] [Google Scholar]
  77. Verdaguer J. Juvenile retinal detachment. Pan American Association of Ophthalmology and American Journal of Ophthalmology Lecture. Am J Ophthalmol. 1982 Feb;93(2):145–156. [PubMed] [Google Scholar]
  78. Wieacker P., Wienker T. F., Dallapiccola B., Bender K., Davies K. E., Ropers H. H. Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Hum Genet. 1983;64(2):143–145. doi: 10.1007/BF00327111. [DOI] [PubMed] [Google Scholar]
  79. Yamaguchi K., Hara S. Autosomal juvenile retinoschisis without foveal retinoschisis. Br J Ophthalmol. 1989 Jun;73(6):470–473. doi: 10.1136/bjo.73.6.470. [DOI] [PMC free article] [PubMed] [Google Scholar]
  80. Yanoff M., Kertesz Rahn E., Zimmerman L. E. Histopathology of juvenile retinoschisis. Arch Ophthalmol. 1968 Jan;79(1):49–53. doi: 10.1001/archopht.1968.03850040051014. [DOI] [PubMed] [Google Scholar]
  81. Yassur Y., Nissenkorn I., Ben-Sira I., Kaffe S., Goodman R. M. Autosomal dominant inheritance of retinoschisis. Am J Ophthalmol. 1982 Sep;94(3):338–343. doi: 10.1016/0002-9394(82)90359-2. [DOI] [PubMed] [Google Scholar]
  82. de Jong P. T., Zrenner E., van Meel G. J., Keunen J. E., van Norren D. Mizuo phenomenon in X-linked retinoschisis. Pathogenesis of the Mizuo phenomenon. Arch Ophthalmol. 1991 Aug;109(8):1104–1108. doi: 10.1001/archopht.1991.01080080064029. [DOI] [PubMed] [Google Scholar]
  83. van Schooneveld M. J., Miyake Y. Fundus albipunctatus-like lesions in juvenile retinoschisis. Br J Ophthalmol. 1994 Aug;78(8):659–661. doi: 10.1136/bjo.78.8.659. [DOI] [PMC free article] [PubMed] [Google Scholar]

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