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TWO PEDIGREES OF HEREDITARY ATAXIA Nariyoshi Yamaguchi 1 , Koroku Negishi 1 , Itsuaki Nakamura 1 , Koji Masahashi 1 , Masaomi Endo 1 , Katsumi Ando 1 1Department of Neuropsychiatry, Kanazawa University School of Medicine pp.17-26
Published Date 1959/1/1
DOI https://doi.org/10.11477/mf.1406200743
  • Abstract
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Recently we examined the two pedigrees which produced patients with hereditary ata-xia in great numbers owing to their consan-guineous marriage.

The results are as follows: 1. In the first pedigree, an in-patient M. U. and ten others (her great-grandfather, her father, a cousin of her father's, an uncle, an aunt, a brother and four cousins on her paternal side) were victims of the same disease through five generation.

2. The in-patient M. U. who has been com-plaining of a disturbance of gait from her forties onward, showed such clinical sympotms as astigmatismus compositus myopicus, eso-phoria, horizontal- and vertical-nystagmus, hyperactivity of tendon reflexes and atactic gait at entering our hospital, and she is living at 48 years old.

3. In the second pedigree, another in-patient I. Y. and five others (his great-grandfather, his grand mother, an uncle, an aunt and mother on his maternal side) were victims of the above-mentioned disease.


Copyright © 1959, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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