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Vogt-Koyanagi-Harada disease developed in monozygotic twins Shinobu Itoh 1 , Itsuko Sugihara 1 , Toshihiko Kouno 2 , Shinji Kurimoto 1 1Dept of Ophthalmol, Yamaguchi Univ Med Sch 2Dept of Ophthalmol, Kyushyu Univ Med Sch pp.125-128
Published Date 1989/2/15
DOI https://doi.org/10.11477/mf.1410210603
  • Abstract
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A 32-year-old female presented with characteris-tic features of Harada disease. Seven years later, her sister developed the same disease at 39 years of age. Both were monozygotic twins.

Papilledema was the prevalent initial clinical feature in both cases. The disease followed a short -termed and favorable course in the former and a protracted course in the latter. The difference in the clinical course seemed to be mainly due to difference in modality of treatment. Both cases showed same HLA types of A2, A26, B51, B7, CW7, DR1 and DR4.

To our best knowledge, this is the first descrip-tion of occurrence of Harada disease in mon-ozygotic twins.


Copyright © 1989, 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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