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Keratoglobus in Down's syndrome. Report of a case Makoto Okuda 1 , Yoshinori Iwama 1 , Jun Takigawa 1 , Mitsuru Sugimoto 1 , Yukitaka Uji 1 1Dep of Ophthalmol, Sch of Med, Mie Univ pp.1769-1772
Published Date 1989/10/15
DOI https://doi.org/10.11477/mf.1410211037
  • Abstract
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A 33-year-old female presented with clinical manifestations of Down's syndrome and keratog-lobus. The keratoglobus was characterized by bilaterality, very small radius of corneal curvature at less than 5.6 mm, and very deep anterior cham-ber depth at 4.6 and 4.8 mm each. Keratoconus could be ruled out on account of uniform andreduced corneal thickness, very low ocular rigidity and absence of Fleischer's ring in the cornea. The endothelial cell population in the central cornea was normal in the left eye and was reduced in the right. The loss of endothelial cells seemed to be the consequence of an earlier episode of acute hydrops in the right eye.


Copyright © 1989, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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