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Japanese

XY PURE GONADAL DYSGENESIS Hidenori Sumiya 1 , Yoshio Shiseki 1 , Jun Shimazaki 1 , Tetsuo Nishikawa 2 , Hisashi Yoshida 2 , Hiroaki Kimura 3 1Department of Urology, Chiba University School of Medicine 2Department of 2nd Internal Medicine, Chiba University School of Medicine 3Department of Obstetrics and Gynecology, Chiba University School of Medicine Keyword: 性分化異常 , 男性半陰陽 pp.72-74
Published Date 1991/1/20
DOI https://doi.org/10.11477/mf.1413900244
  • Abstract
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We report a case of XY pure gonadal dysgenesis in a 24-year-old registered woman, who complained of primary amenorrhea. Chromosomal analyses revealed a 46 XY by G-banding, a presence of Y-body by Q -banding and all the Y-originating fragments by DNA probe hybridization. Endocrinologically both LH and FSH were markedly elevated and no testosterone increase was observed by hCG stimulation. Laparotomy revealed a vestigial uterus and no gonad.


Copyright © 1991, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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