Primary Hereditary Oxalosis Retinopathy
- 1 January 1983
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 101 (1) , 78-80
- https://doi.org/10.1001/archopht.1983.01040010080013
Abstract
• A female infant had progressive atypical pigmentary retinopathy with type 1 hereditary oxalosis. At the age of 3 months she had a flecked retina type of retinopathy and six months later she exhibited a unique type of atypical pigmentary retinopathy. This latter abnormality was characterized by a dense parafoveal hyperpigmented ring five disc diameters in size, and composed of a confluence of small rings of hyperpigmented retinal pigment epithelium surrounding whitish highly refractile calcium oxalate crystalline deposits.Keywords
This publication has 3 references indexed in Scilit:
- Fluorescein Angiography and Vitamin a and Oxalate Levels in Fundus AlbipunctatusAmerican Journal of Ophthalmology, 1976
- Flecked RetinaArchives of Ophthalmology (1950), 1975
- Alterations of Pigment Epithelium in CystinosisArchives of Ophthalmology (1950), 1967