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Japanese

A FAMILY OF JUVENILE RETINOSCHISIS Takehisa Saito 1 , Yuya Satoh 1 , Teruo Seimiya 1 , Naoya Koda 1 , Itsuo Asamizu , Toshio Mori 2 1Department of Ophthalmology, School of Medicine, Tohoku University 2Aomori Rosai Hospital pp.849-856
Published Date 1971/3/15
DOI https://doi.org/10.11477/mf.1410204522
  • Abstract
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A pedigree in which five young males areaffected by retinoschisis and their grand father suspected retinoschisis from family history is reported.

Common clinical manifestations were eleva-tion of temporal periphery in the retina, large oval holes in the internal layer of the retina and macular degeneration. Other findings were translucent membrane projecting into the vitre-ous (case 1), chorioretinal atrophy with and without granular pigmentation (case 1, 2), disc distortion similar to retinopathy in premature (case 3), dendritic retinal markings (case 2) and history of vitreous haemorrhage.


Copyright © 1971, 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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