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Japanese

A pedigree of Goldmann-Favre disease Yoshihiko Yonekura 1 , Masao Tamaki 1 , Yoshihide Nakai 1 , Hiroyuki Takashiba 1 1Department of Ophthalmology, Mie University School of Medicine pp.431-436
Published Date 1978/3/15
DOI https://doi.org/10.11477/mf.1410207613
  • Abstract
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A 23-year-old male and his 19-year-old sister, offsprings of consanguineous marriage of apparently normal parents, developed visual impairment and night blindness since adolescence. They showed fibrillar vitreous opacities, cystic macular degene-ration and atypical pigmentary retinopathies. Stereofunduscopy and slitlamp examination re-vealed the characteristic macular change to be due to a fibrous network intervening between the pre-retinal vitreous membrane and the retinal surface without causing true cystic formation. The observed fibrous network seemed to be in contact with the component of nerve fiber layer.


Copyright © 1978, 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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