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Japanese

A case of Rieger's syndrome Eiichi Hasegawa 1 , Nobuhiko Matsuo 1 , Osamu Kumashiro 1 , Nozomu Katayama 1 1Department of Ophthalmology, Okayama Univresity Medical School pp.1179-1183
Published Date 1979/8/15
DOI https://doi.org/10.11477/mf.1410207951
  • Abstract
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A 16-year-old boy manifested typical clinicalfeatures of mesodermal dysgenesis of the anterior segment (Rieger's syndrome). There was hypo-plasia of the anterior iris leaf and an anomaly of the anterior chamber angle. The intraocular pressure was grossly elevated. There were extra-ocular involvements as neural hearing loss, dental and skeletal anomalies. This case did not belong neither to the type I or II as classified by Ta-kahashi as it showed the mixed type. We per-formed trabeculectomy for the right eye. Ten months after surgery, the visual functions remain satisfactory with topical pilocarpine and epine-phrine.


Copyright © 1979, 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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