Oculomotor Behavior in Human Albinos

  • P. Apkarian
  • H. Spekreijse
  • H. Collewijn
Part of the Documenta Ophthalmologica Proceedings Series book series (DOPS, volume 37)

Abstract

In a recent visual evoked potential (VEP) investigation (Apkarian et al., 1982), asymmetry in the monocular VEP, reflecting abnormal retino-geniculocortical projections, was detected in all albinos with measurable responses and with zero false positives in non-albino controls. In contrast to monocular VEP asymmetry, oculomotor disturbances such as nystagmus, an established albino concomitant, are neither a specific nor an obligate albino pathognomonic. Because not all albinos demonstrate oculomotor disturbances whereas non-albinos may, the link between aberrant projections and organization of the oculomotor control centers in these patients is at question. To address this problem we have examined spontaneous eye movements, simultaneously recorded during VEP measurements, and stimulus induced optokinetic nystagmus (OKN) in albinos with nystagmus, an albino without nystagmus and a non-albino with nystagmus. As an objective confirmation of the clinical diagnosis, all subjects tested in this investigation were screened for VEP albino asymmetry. Simultaneously recorded EOGs indicated curious disjunctive eye movements; under certain conditions, the amplitude of the movement of one eye was significantly greater than that of the other eye. With OKN recordings, examined with both full-field and half-field conditions as a function of direction of target motion, inverted OKN was observed for an albino observer as well as for the non-albino control. One albino who did not show inverted OKN under any conditions, did show OKN directional asymmetry during partial-field stimulation. The variable OKN response patterns observed in our subject sample indicate that OKN disturbances, particularly inverted OKN and OKN directional asymmetry, necessitate further investigation to determine the relationship between aberrant retinal fiber projections and oculomotor control.

Keywords

Target Motion Visual Evoke Potential Fast Phase Optokinetic Nystagmus Monocular Deprivation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Apkarian, P., Reits, D., Spekreijse, H. and Dorp, D. van. A decisive electrophysiological test for human albinism. Electroenceph. clin. Neurophysiol. (submitted) 1982.Google Scholar
  2. Atkinson, J. Development of optokinetic nystagmus in the human infant and infant monkey: an analogue to development in kittens. In: Freeman, R. H. (ed.) Developmental Neurobiology of Vision, 277–287, Plenum Press, New York, 1979.Google Scholar
  3. Baloh, R. W., Yee, R. D. and Honrubia, V. Optokinetic asymmetry in patients with maldeveloped foveas. Brain Res. 186: 210–216, 1980.CrossRefGoogle Scholar
  4. Bergsma, D. Birth Defects, Atlas and Compendium. The National Foundation. White Plains, New York, 1973.Google Scholar
  5. Coleman, J., Sydnor, C. F., Wolbarsht, M. L. and Bessler, M. Abnormal visual pathways in human albinos studied with visually evoked potentials. Exp. Neurol. 65: 667–679, 1979.PubMedCrossRefGoogle Scholar
  6. Collewijn, H. Optokinetic eye movements in the rabbit: input-output relations. Vision Res. 9: 111–132, 1969.Google Scholar
  7. Collewijn, H. Eye- and head movements in freely moving rabbits. J. Physiol. 266: 471–498, 1977.PubMedGoogle Scholar
  8. Collewijn, H., Winterson, B. J. and Dubois, M. F. W. Optokinetic eye movements in albino rabbits: inversion in anterior visual field. Science 199: 1351–1353, 1978.PubMedCrossRefGoogle Scholar
  9. Collewijn, H. Mark, F. van der, Jansen, T. C. Precise recording of human eye movements. Vision Res. 15: 447–450, 1975.PubMedCrossRefGoogle Scholar
  10. Creel, D., Hendrickson, A. E. and Leventhal, A. G. Retinal projection in tyrosinase-negative albino cats. J. Neurosci. 2: 907–911, 1982.PubMedGoogle Scholar
  11. Creel, D., Spekreijse, H. and Reits, D. Evoked potentials in albinos: efficacy of pattern stimuli in detecting misrouted optic fibers. Electroenceph. clin. Neurophysiol. 52: 595–603, 1981.PubMedCrossRefGoogle Scholar
  12. Duke-Elder, S. System of opthalmology, vol. 3 Normal and abnormal development, part 2 Congenital deformities. Mosby, St. Louis, Mo. 1963, 803–813.Google Scholar
  13. Giolli, R. A. and Creel, D. J. The primary optic projections in pigmented albino guinea pigs: an experimental degeneration study. Brain Res. 55: 25–39, 1973.PubMedCrossRefGoogle Scholar
  14. Gross, K. J. and Hickey, T. L. Abnormal laminar patterns in the lateral geniculate nucleus of an albino monkey. Brain Res. 190: 231–237, 1980.PubMedCrossRefGoogle Scholar
  15. Guillery, R. W. and Kaas, J. H. A study of normal and congenitally abnormal retinogeniculate projections in cats. J. Comp. Neurol. 143: 73–100, 1971.PubMedCrossRefGoogle Scholar
  16. Guillery, R. W. and Kaas, J. H. Genetic abnormality of visual pathways in a ‘white’ tiger. Science 180: 1287–1289, 1973.PubMedCrossRefGoogle Scholar
  17. Guillery, R. W., Okoro, A. N. and Witkop, C. J. Jr. Abnormal visual pathways in the brain of a human albino. Brain Res. 96: 373–377, 1975.PubMedCrossRefGoogle Scholar
  18. Hoffman, K. P. Optokinetic nystagmus and single-cell responses in the nucleus tractus opticus after early monocular deprivation in the cat. In: Freeman, R. H. (ed.) Developmental Neurobiology of Vision, 63–72, Plenum Press, New York, 1979.Google Scholar
  19. Julesz, B. Binocular depth perception without familiarity cues. Science 145: 356–362, 1964.PubMedCrossRefGoogle Scholar
  20. Krill, A. E. Hereditary Retinal and Coroidal Diseases. Vol. II Clinical Characteristics, Harper and Row Publ. Hagerstown, Maryland, 1977, 645–664.Google Scholar
  21. Lund, R. D. Uncrossed visual pathways in hooded and albino rats. Science 149: 1506–1509, 1965.PubMedCrossRefGoogle Scholar
  22. Mowrer, O. H. A comparison of the reaction mechanisms mediating optokinetic nystagmus in human beings and in pigeons. Psychol. Monogr. 47: 294–305, 1936.CrossRefGoogle Scholar
  23. Precht, W., Cazin, L. Functional deficits in the optokinetic system of albino rats. Exp. Brain Res. 37: 183–186,1979.PubMedCrossRefGoogle Scholar
  24. Schor, C. M. and Levi, D. M. Disturbances of small-field horizontal and vertical optokinetic nystagmus in amblyopia. Invest. Ophthalmol. Vis. Sci. 19: 668–683, 1980.PubMedGoogle Scholar
  25. Smith, K. U. and Bridgeman, M. The neural mechanisms of movement vision and optic nystagmus. J. Exp. Psychol. 33: 165–187, 1943.CrossRefGoogle Scholar
  26. Spekreijse, H., Tweel, H. van der and Zuidema, Th. Contrast evoked responses in man. Vision Res. 13: 1577–1601, 1973.PubMedCrossRefGoogle Scholar
  27. Van Die, G. and Collewijn, H. Optokinetic nystagmus in man. Role of central and peripheral retina and occurance of asymmetries. Human Neurobiol. 1: 111–119, 1982.Google Scholar
  28. Van Hof-van Duin, J. Early and permanent effects of monocular deprivation on pattern discrimination and visumotor behavior in cats. Brain Res. 111: 261–276, 1976.PubMedCrossRefGoogle Scholar
  29. Wakusawa, S. and Sato, Y. Development of optokinetic response in the human infant. Jap. J. Ophthalmol. 18: 299–310, 1974.Google Scholar
  30. Weber, J. T., Kaas, J. H. and Harting, J. K. Retinocollicular pathways in Siamese cats: an autoradiographic analysis. Brain Res. 148: 189–196, 1978.PubMedCrossRefGoogle Scholar
  31. Wildberger, H. and Meyer, M. Zur augenmotorischen Störung des Albino. Klin. Monatsbl. Augenheilk. 172: 487–490, 1978.Google Scholar
  32. Wood, C. C., Spear, P. D. and Braun, J. J. Direction-specific deficits in horizontal optokinetic nystagmus following removal of visual cortex in the cat. Brain Res. 60: 231–237, 1973.PubMedCrossRefGoogle Scholar

Copyright information

© Dr. W. Junk 1983

Authors and Affiliations

  • P. Apkarian
    • 1
    • 2
  • H. Spekreijse
    • 1
    • 2
  • H. Collewijn
    • 1
    • 2
  1. 1.AmsterdamThe Netherlands
  2. 2.RotterdamThe Netherlands

Personalised recommendations