Retinal detachment in a case of homocystinuria

T. Noda, S. Abe, Y. Ando, K. Shimizu, M. Tani, K. Negishi, K. I. Akiyama

研究成果: Article査読

抄録

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.

本文言語English
ページ(範囲)23-27
ページ数5
ジャーナルJapanese Journal of Clinical Ophthalmology
50
1
出版ステータスPublished - 1996
外部発表はい

ASJC Scopus subject areas

  • 眼科学

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