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Japanese

Juvenile uveitis characterized by recurrent iritis, secondary drusen and retinal vasculitis Yuichiro Ogura 1 , Satoshi Okinami 1 , Nobuchika Ogino 1 1Department of Ophthalmology, Faculty of Medicine, Kyoto University pp.55-61
Published Date 1982/1/15
DOI https://doi.org/10.11477/mf.1410208506
  • Abstract
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Two females, aged 15 and 17 years each, develop-ed uveitis of unknown etiology with some distinct clinical features. The condition occurred as bilate-ral recurrent mild iritis associated with retinal flecks and peripheral retinal vasculitis. The flecks were yellowish-gray in color, punctate, sharply defined, and were located in the pigment epithelial layer. Some were irregularly confluent. They were dis-tributed mainly in the equatorial region and were absent in the macula. On fluorescein angiography, they appeared as hyperfluorescent spots showing pigment epithelial window defect.


Copyright © 1982, 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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