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Japanese

Retinal Dysplasia: Report of two cases Hisaharu Yoshioka 1 , Kinichi Hirose 1 1Department of Ophthalmology, Kurume University, School of Medicine pp.128-134
Published Date 1964/2/15
DOI https://doi.org/10.11477/mf.1410202879
  • Abstract
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The case 1 (four month old, female) was enucleated because of leukokoria of the right eye and suspected retinoblastoma. Histologica-lly retinal dysgenesis with retinal rosette, persistence of primary vitreous, retinal deta-chment, foetal angle, elongation of ciliary process, subretinal hemorrhage and preretinal glial structure were observed. From the abo-ve findings, the author concluded that a close relationship exists between the persistent hyperplastic primary vitreous and retinal dy-splasia.

The case 2 (full term stillbirth, female) showed microphthalmos, shallow anterior cha-mber, coloboma of iris, and leukokoria.


Copyright © 1964, 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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