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Two cases of cone-rod dystrophy with spinocerebellar degeneration Motozumi Itoi 1 , Mutsuko Hayakawa 1 , Hitoshi Sakuma 1 , Kenji Yanashima 2 , Tomoyoshi Kondo 3 , Yukihiro Sugita 3 , Katsunori Nishi 3 , Atsushi Kanai 1 1Dept of Ophthalmol, Juntendo Univ Sch of Med 2Dept of Ophthalmol, National Rehabil Center 3Dept of Neurology, Juntendo Univ Sch of Med pp.225-230
Published Date 1993/2/15
DOI https://doi.org/10.11477/mf.1410901467
  • Abstract
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We report two cases of cone-rod dystrophy with spinocerebellar degeneration. The first case, a 48 -year-old female with familial involvement, show-ed slight temporal pallor of the disc with narrowing of retinal arteries in both eyes. The second case, a 45-year-old female without familial trait, showed circular atrophy with white dots in the macular area. The midperipheral fundus showed faint gran-ular pigmentation in both eyes. The findings were inconsistent with the hitherto known descriptions of cone-rod dystrophy with spinocerebellar degen-eration. We emphasize that atypical cone-rod degeneration may be associated with spinocerebel-lar degeneration.


Copyright © 1993, 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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