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Japanese

Gyrate atrophy of the choroid and retina Hisao Nakajima 1 , Seiji Hayasaka 1 , Yoichi Takaku 1 , Takashi Shiono 1 , Seiichi Watanabe 1 , Jinkichi Takahashi 1 , Katsuyoshi Mizuno 1 , Shun Saito 2 , Kiyoshi Omura 2 , Keiya Tada 2 1Department of Ophthalmology, Tohoku University School of Medicine 2Department of Pediatrics, Tohoku University School of Medicine pp.961-968
Published Date 1981/6/15
DOI https://doi.org/10.11477/mf.1410208372
  • Abstract
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Four cases of gyrate atrophy were investigated clinically and biochemically. Three cases showed chorioretinal atrophy, characterized by spotty cho-roidal atrophy which had tendency to confluent, and which showed hypofluorescent patches bound-ed by a hyperfluorescent line. A 5-year-old boy who initially lacked typical fundus changes but showed hyperornithinemia developed small atrophic patches in the equator 2 years later. Electrophysio-logical responses including ERG and EOG were extinct or subnormal in all cases.


Copyright © 1981, 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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