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Short wavelength-automated perimetry compared with standard achromatic perimetry in autosomal dominant optic atrophy
  1. J W Walters,
  2. A Gaume,
  3. L Pate
  1. University of Houston, Houston, Texas, USA
  1. Correspondence to: J W Walters College of Optometry, University of Houston, J Davis Armistead Building, Houston, Texas 77204-6052, USA; dr_jimwalters{at}yahoo.com

Abstract

Background: Autosomal dominant optic atrophy (ADOA, Kjer-type) is a heterogeneous, non-inflammatory degeneration of retinal ganglion cells. The diagnosis of ADOA can be challenging owing to its insidious onset and large variability in phenotypic expression, both within and between individual pedigrees. The earliest literature reports relatively mild centrocaecal scatomas to white targets in ADOA, but extensive and dense peripheral field loss to coloured targets, especially blue, with Bjerrum perimetry. The phrase “inverted peripheral visual fields to coloured targets” has been used to describe this phenomenon.

Methods: Humphrey standard achromatic perimetry (SAP) and short wavelength-automated perimetry (SWAP) were carried out on five patients with ADOA.

Results: Regardless of wide variations in patient age, visual acuity, disc appearance and colour vision, the SWAP mean deviation (MD) was between 10 and 20 times more depressed than the SAP MD. The actual differences ranged from 9.38 to 13.78 dB.

Conclusions: These data are consistent with the original reports suggesting that, early in this disease process, the blue-target deficits are typically peripheral and that this difference between SAP and SWAP perimetry may be a robust indicator of ADOA in both early and late stages of this disease.

  • ADOA, autosomal dominant optic atrophy
  • BVA, best-corrected visual acuity
  • NTG, normal tension glaucoma
  • SAP, standard achromatic perimetry
  • SWAP, short wavelength-automated perimetry

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Footnotes

  • Competing interests: None declared.

  • Published Online First 12 July 2006

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