Autosomal dominant vitreoretinochoroidopathy (ADVIRC)

N. P. Blair, M. F. Goldberg, G. A. Fishman, T. Salzano

Research output: Contribution to journalArticlepeer-review

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°, 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.

Original languageEnglish (US)
Pages (from-to)2-9
Number of pages8
JournalBritish Journal of Ophthalmology
Volume68
Issue number1
DOIs
StatePublished - 1984
Externally publishedYes

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

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