Abstract
A 16-year-old boy had a central retinal artery occlusion and was subsequently diagnosed as a hemizygote with Fabry's disease. The typical ocular manifestations in males with this inborn error of glycosphingolipid metabolism include whorl-like corneal epithelial infiltrates, retinal and conjunctival vessel tortuosity, and lenticular changes. The present case represents the first report of a retinal artery occlusion as an ocular complication of Fabry's disease.
| Original language | English |
|---|---|
| Pages (from-to) | 815-817 |
| Number of pages | 3 |
| Journal | Archives of Ophthalmology |
| Volume | 96 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 1978 |