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Japanese

A Case of Retinal Dysplasia. Takashi Nakagawa 1 , Tetuo Ito 2 1Department of Ophthalmology, Sapporo Medical College. 2Department of Pathology, Sapporo Municipal Hospital. pp.1379-1382
Published Date 1965/11/15
DOI https://doi.org/10.11477/mf.1410203300
  • Abstract
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The patient was a 2 month old male born at full term with non-contributory family history.

It had bilateral leukokoria. Ophthalmic exa-mination revealed that both eyes had retro-lental membranes which appeared to be scar-cely vascularized. Histologically both eyes were the same. Both showed the total reti-nal detachment except the pigment layer. Detached retina developed into the prolifera-tive infolding with typical rosettes and per-sistence of the primary vitreous. Chamber angles were almost normal. Impaired speech was observed by the time the patient was 3 years old.


Copyright © 1965, 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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