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Retinal Detachment in a case of homocystinuria Toru Noda 1 , Satoru Abe 1 , Yuko Ando 1 , Keiichiro Shimizu 1 , Mizuko Tani 1 , Kazuno Negishi 2 , Ken-ichi Akiyama 3 1Dept of Ophthalmol, The Second Tokyo National Hosp 2Dept of Ophthalmol, National Saitama Hosp 3Akiyama Eye Clinic pp.23-27
Published Date 1996/1/15
DOI https://doi.org/10.11477/mf.1410904705
  • Abstract
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A 21-year-old male presented with bilateral lens dislocation. He showed skeletal abnormalities simulating Marfan syndrome, mental retardation and history of convulsion during childhood. He was diagnosed as homocystinuria by laboratory studies. After five years of follow-up, rhegmatogenous retinal detachment developed in the right eye, which was brought to cure by multiple surgeries. Retinal detachment in homocystinuria was difficult to detect and treat because of concomitant systemic and mental problems.


Copyright © 1996, 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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