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A case of pigmentary dispersion syndrome Hiroe Uto 1 , Hideo Araki 1 , Shigeru Sugai 1 , Hajime Inomata 1 1Dept of Ophthalmol, Fac of Med, Kyushu Univ pp.183-186
Published Date 1990/2/15
DOI https://doi.org/10.11477/mf.1410900036
  • Abstract
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A 37-year-old Japanese male was referred to usunder the tentative diagnosis of bilateral uveitisand central retinal vein occlusion in the left eye.Both eyes showed deposition of pigment granuleson the posterior corneal surface simulating Kruken-berg's spindle, on the lens and the trabecular me-shwork. No radial transillumination defects wereseen in the iris. Signs of glaucoma were consistentlyabsent. This case illustrates that pigment disper-sion syndrome may develop in the Japanese as arare occurrence.


Copyright © 1990, 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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