Retinal detachment in a case of homocystinuria

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

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Abstract

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.

Original languageEnglish
Pages (from-to)23-27
Number of pages5
JournalJapanese Journal of Clinical Ophthalmology
Volume50
Issue number1
Publication statusPublished - 1996 Jan 1

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ASJC Scopus subject areas

  • Ophthalmology

Cite this

Noda, T., Abe, S., Ando, Y., Shimizu, K., Tani, M., Negishi, K., & Akiyama, K. I. (1996). Retinal detachment in a case of homocystinuria. Japanese Journal of Clinical Ophthalmology, 50(1), 23-27.