Reis-Bückler’s Dystrophy

  • Y. Pouliquen
  • J. P. Giraud
  • M. Savoldelli
Conference paper
Part of the Current Research in Ophthalmic Electron Microscopy book series (CR OPHTHALMIC, volume 2)

Summary

A case of Reis-Bückler’s dystrophy in a 36-year-old man is reported. Its clinical aspect is compared with its histological and ultrastructural features. The slight reticular opacities situated superficially in the central part of the cornea, immediately beneath the epithelium, correspond to dark, irregular deposits. These replaced the basal membrane and Bowman’s membrane and are composed of granular material, glycogen granules, and short fibers. These short, curved, osmiophilic fibers whose diameter is approximately 130 A are also located inside the anterior stromal lamellae. These deposits seem to be the characteristic feature of this particular and rare dystrophy, stated as by Hogan. Their nature and origin are discussed.

Keywords

Retina Paraffin Fibril Glutaraldehyde Reticulin 

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References

  1. 1.
    Akiya, S., Brown, S.I.: The ultrastructure of Reis-Bückler’s dystrophy. Amer. J. Ophthal. 72, 549–554 (1971)PubMedGoogle Scholar
  2. 2.
    Babel, J., Leuenberger, P.: Corneal dystrophy of Reis-Bückler’s. Ultrastructure study of two cases. Arch. Ophthal. Paris 33, 49–62 (1973)Google Scholar
  3. 3.
    Hogan, M.J.: Patogenia de la distrofia corneal de Reis-Bückler. Arch. Soc. Esp. Oftal. 37, 109- (1977)Google Scholar
  4. 4.
    Kanai, A., Kaufmann, H.E., Polak, F.M.: Electron microscopic study of Reis-Bückler’s dystrophy. Amer. J. Ophthal. 5, 953 (1973)Google Scholar

Copyright information

© Springer-Verlag Berlin · Heidelberg 1978

Authors and Affiliations

  • Y. Pouliquen
    • 1
  • J. P. Giraud
    • 1
  • M. Savoldelli
    • 1
  1. 1.Laboratoire de la Clinique Ophtalmologique de l’Hôtel DieuParis Cedex 04France

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