Visual evoked potentials with crossed asymmetry in incomplete congenital stationary night blindness

Investigative Ophthalmology and Visual Science

Volumn 37, Issue 9, 1996, Pages 1783-1792

  Tremblay, François ^a,b   De Becker, Inge ^a   Cheung, Cindy ^a   LaRoche, G Robert ^a  

^a DALHOUSIE UNIVERSITY   (Canada)

^b Izaak Walton Killam Hospital for Children   (Canada)

Author keywords

albinism; CSNB2; optic chiasm; retinal degeneration; retinal ganglion cells; visual evoked potentials

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; FEMALE; HUMAN; MALE; NIGHT BLINDNESS; OCULAR ALBINISM; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ALBINISM, OCULAR; CHILD; CHILD, PRESCHOOL; ELECTRORETINOGRAPHY; EVOKED POTENTIALS, VISUAL; FEMALE; HUMANS; INFANT; MALE; NIGHT BLINDNESS; NORMAL DISTRIBUTION; OSCILLOMETRY; REFERENCE VALUES; VISUAL ACUITY;

EID: 0029812550     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (44)

1. Tremblay F, LaRoche RG, De Becker I. The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness. Vision Res. 1995; 35:2383-2393.
2. Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T. Congenital stationary night blindness with negative electroretinogram: A new classification. Arch Ophthalmol. 1986; 104:1013-1020.
3. Miyake Y. Incomplete type congenital stationary night blindness. In: Heckenlively JR, Arden GB, eds. Principles and Practice of Clinical Electrophysiology of Vision. St. Louis: CV Mosby; 1991:721-725.
4. Apkarian P, Shallo-Hoffmann J. VEP projections in congenital nystagmus; VEP asymmetry in albinism: A comparison study. Invest Ophthalmol Vis Sci. 1991; 32:2653-2661.
5. Kriss A, Timms C, Elston, Taylor D, Gresty M. Visual evoked potentials in dissociated vertical deviation: a reappraisal. Br J Ophthalmol. 1989; 73:265-270.
6. Boylan C, Clement CA, Howrie A. Normal visual pathway routing in dissociated vertical deviation. Invest Ophthalmol Vis Sci. 1988;29:1165-1167
7. Bach M, Kommerell G. Albino-type misrouting of the optic nerve fibers not found in dissociated vertical deviation. Graefe's Arch Clin Exp Ophthalmol. 1992; 230:158-161.
8. Roy S. Prader-Willi syndrome: A clinical and visually evoked potential study. ARVO Abstracts. Invest Ophthalmol Vis Sci. 1991; 32:761.
9. Apkarian P, Reits D, Spekreijse H, van Dorp D. A decisive electrophysiological test for human albinism. Electroencephalogr Clin Neurophysiol. 1983;55:513-531.
10. Russell-Eggitt I, Kriss A, Taylor DSI. Albinism in childhood: A flash VEP and ERG study. Br J Ophthalmol. 1990;74:136-140.
11. Bouzas E, Caruso RC, Drews-Bankiewicz MA, Kaiser-Kupfer MI. Evoked potential analysis of visual pathways in human albinism. Ophthalmology. 1994; 101:309-314.
12. Guo S, Reinecke RD, Fendick M, Calhoun JH. Visual pathway abnormalities in albinism and infantile nystagmus: VECPs and stereoacuity measurements. J Pediatr Ophthalmol Strabismus. 1989;26:97-104.
13. Carroll WM, Jay BS, McDonald WI, Halliday AM. Two distinct patterns of visual evoked response asymmetry in human albinism. Nature. 1980;286:604-606.
14. Meienberg O, Hemphill G, Rosenberg M, Hoyt WF. Visually evoked response asymmetries in a family with congenital nystagmus. Arch Neurol. 1980;37:397-402.
15. Fitzgerald BA, Billson FA. Dissociated vertical deviation: Evidence of abnormal visual pathway projection. Br J Ophthalmol. 1984;68:801-806.
16. Krill AE, Martin D. Photopic abnormalities in congenital stationary nightblindness. Invest Ophthalmol Vis Sci. 1971;10:625-636.
17. Regan D. Human Brain Electrophysiology. Amsterdam: Elsevier; 1989:548-552.
18. Leventhal A, Vitek DJ, Creel DJ. Abnormal visual pathways in normally pigmented cats that are heterozygous for albinism. Science. 1985;220:1395-1396.
19. Jeffery G, Darling K, Whitmore A. Melanin and the regulation of mammalian photoreceptor topography. Eur J Neurosci. 1994;6:657-667.
20. Guillery RW. Neural abnormalities of albinos. Trends Neurosci. 1986;9:366-369.
21. Sretavan DW. Specific routing of retinal ganglion cell axons at the mammalian optic chisasm during embryonic development. J Neurosci. 1990;10:1995-2007.
22. Drager UC. Birthdates of retinal ganglion cells giving rise to the crossed and uncrossed optic projection in the mouse. Proc R Soc Lond B Biol Sci. 1985;224:57-77.
23. LaVail JH, Nixon RA, Sidman RL. Genetic control of retinal ganglion cell projections. J Camp Neurol. 1978;182:399-422.
24. Colello RJ, Jeffery G. Evaluation of the influence of optic stalk melanin on the chiasmatic pathways in the developing rodent visual system. J Comp Neurol. 1991;305:304-523.
25. Silver J, Sapiro J. Axonal guidance during development of the optic nerve: the role of pigmented epithelia and other extrinsic factors. J Comp Neurol. 1981;202:521-538.
26. Kinnear PE, Jay B, Witkop CJ. Albinism. Surv Ophthalmol. 1985;30:75-101.
27. Abadi RV, Pascal E. Visual resolution limits in human albinism. Vision Res. 1991;7/8:1445-1447.
28. Kellner U, Foester MH. Cone dystrophies with negative electroretinogram. Br J Ophthalmol. 1993;77:404-409.
29. Perlman I, Leibu R, Barth J. Night blindness: A new type with abnormal properties of the electroretinogram. Clin Vision Res. 1993;8:159-169.
30. Tremblay F, De Becker I, Dooley JM, Riddell DC. Duchenne muscular dystrophy: Negative scotopic bright-flash electroretinogram but not congenital stationary night blindness. Can J Ophthalmol. 1994; 29:274-279.
31. Jensen H, Warburg M, Sjö O, Schwartz M. Duchenne muscular dystrophy: Negative electroretinograms and normal dark adaptation: Reappraisal of assignment of X linked incomplete congenital stationary night blindness. JMed Genet. 1995;32:348-351.
32. Peachey NS, Fishman GA, Derlaki DJ, Bringell MG. Psychophysical and electroretinographic findings in X-Linked juvenile retinoschisis. Arch Ophthalmol. 1987; 105:513-516.
33. Wack MA, Peachey NS, Fishman GA. Electroretinographic findings in human oculocutaneous albinism. Ophthalmology. 1989;96:1778-1785.
34. Krill A. Congenital stationary night blindness. In: Krill's Hereditary Retinal and Choroidal Diseases. Vol. II. New York: Harper & Row; 1977:391-420.
35. Rosenberg T, Schwartz M, Simonsen SE. Aland eye disease (Forsius-Eriksason-Miyake syndrome) with probability established in a Danish family. Acta Ophthalmol. 1990;68:281-291.
36. Weleber RG, Pillers D-AM, Powell BR, Hanna CE, Magenis RE, Buist NRM. Aland Island eye disease (Forscius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21: Similarity to congenital stationary night blindness. Arch Ophthalmol. 1989; 107:1170-1179.
37. Carlson S, Vesti E, Raitta C, Donner M, Eriksson AW, Forsius H. Clinical and electroretinographic comparison between Åland island eye disease and a newly found related disease with X-chromosomal inheritance. Acta Ophthalmol. 1991;69:703-710.
38. O'Donnell FE, Green WR, McKusick VA, Forsius H, Eriksson AW. Forsius-Eriksson syndrome: Its relation to the Nettleship-Falls X-linked ocular albinism. Clin Genet. 1980;17:403-408.
39. Glass IA, Good P, Coleman MP, Fullwood P, Giles MG, Lindsay S, et al. Genetic mapping of a cone and rod dysfunction (Åland Island eye disease) to the proximal short arm of the human X chromosome. J Med Genet. 1993;30:1044-1051.
40. van Dorp DB, Eriksson AW, Delleman JW, et al. Åland eye disease: No albino misrouting. Clin Genet. 1985; 28:526-530.
41. Pillers D-AM, Bulman DE, Weleber RG, et al. Dystrophin expression in the human retina is required for normal function as defined by electroretinography. Nat Genet. 1993;4:82-86.
42. Alitalo T, Kruse TA, Forsius H, Eriksson AW, de la Chapelle A. Localization of the Åland Island eye disease locus to the pericentric region of the X chromosome by linkage analysis. Am J Hum Genet. 1991;48:31-38.
43. Musarella MA, Weleber RG, Murphey WH, et al. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3. Genomics. 1989;5:727-737.
44. Pearce WG, Reedyk M, Couplan dSG. Variable expressivity in X-linked congenital stationary night blindness. Can J Ophthalmol. 1990;25:3-10.