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. 1984 Jan;68(1):2–9. doi: 10.1136/bjo.68.1.2

Autosomal dominant vitreoretinochoroidopathy (ADVIRC).

N P Blair, M F Goldberg, G A Fishman, T Salzano
PMCID: PMC1040228  PMID: 6689931

Abstract

We report the second family recognised to have autosomal dominant vitreoretinochoroidopathy. The clinical features were (1) autosomal dominant inheritance; (2) peripheral, coarse pigmentary degeneration of the fundus for 360 degrees, with a relatively discrete posterior border in the equatorial region (this finding may be pathognomonic); (3) superficial punctate yellowish-white opacities in the retina; (4) various vascular abnormalities; (5) breakdown of the blood-retinal barrier; (6) retinal neovascularisation; (7) vitreous abnormalities; and (8) choroidal atrophy. Visual reduction was mainly due to macular oedema or vitreous haemorrhage.

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Selected References

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