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A case of congenital total colour-weakness Dosetsu Kanaizuka 1 1Department of Ophthalmology, Chiba University School of Medicine pp.540-544
Published Date 1961/4/15
DOI https://doi.org/10.11477/mf.1410207227
  • Abstract
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Reports of a male aged 19 who was diagnosed to have congenital total colour-weakness by examination using many kinds of pseudoisochromatic plates and type II of the anoma-loscope. In investigation using type II of the anomaloscope, it was matched like deutera-nopia, further it matched at the side of a short wave length, that should not match in the case of deuteranopia. From this result it looks as if trianopia exists, and the conclu-sion of this case was that deuteranopia with tritanopia existed at the same time.


Copyright © 1961, 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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