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Literature DB >> 6849658

Primary hereditary oxalosis retinopathy.

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.

Entities: Chemical Disease Species

Mesh：

Substances：
Oxalates

Year: 1983 PMID： 6849658 DOI： 10.1001/archopht.1983.01040010080013

Source DB: PubMed Journal: Arch Ophthalmol ISSN： 0003-9950

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Cited

5 in total

5. Experimental calcium oxalate retinopathy compared with cystine- and tyrosine-induced retinal damage. An ophthalmoscopical, histological, and electrophysiological study.

Authors: U Weber; H U Sons; R Hennekes; W Lenz
Journal: Graefes Arch Clin Exp Ophthalmol Date: 1986 Impact factor: 3.117

5 in total

Primary hereditary oxalosis retinopathy.

1. Early onset of stone diseases and primary hyperoxaluria.

2. [Type I oxalosis in childhood--studies within the scope of terminal renal failure in the child].

3. A clinicopathological study of ocular involvement in primary hyperoxaluria type I.

4. New aspects of infantile oxalosis.

5. Experimental calcium oxalate retinopathy compared with cystine- and tyrosine-induced retinal damage. An ophthalmoscopical, histological, and electrophysiological study.