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Published in: Documenta Ophthalmologica 2/2008

Open Access 01-03-2008 | Original Research Article

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update

Authors: Anthony G. Robson, Michel Michaelides, Zubin Saihan, Alan C. Bird, Andrew R. Webster, Anthony T. Moore, Fred W. Fitzke, Graham E. Holder

Published in: Documenta Ophthalmologica | Issue 2/2008

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Abstract

Purpose To examine the presence and functional significance of annular fundus autofluorescence abnormalities in patients with different retinal dystrophies. Methods Eighty one patients were ascertained who had a parafoveal ring of high density on fundus autofluorescence imaging. Sixty two had had a clinical diagnosis of retinitis pigmentosa (RP) or Usher syndrome with normal visual acuity. Others included a case of Leber congenital amaurosis and genetically confirmed cases of cone or cone-rod dystrophy (GUCA1A, RPGR, RIMS1), “cone dystrophy with supernormal rod ERG” (KCNV2) and X-linked retinoschisis (RS1). International-standard full-field and pattern electroretinography (ERG; PERG) were performed. Some patients with rod-cone or cone-rod dystrophy underwent multifocal ERG (mfERG) testing and photopic and scotopic fine matrix mapping (FMM). Results In patients with RP, the radius of the parafoveal ring of high density correlated with PERG P50 (R = 0.83, P < 0.0005, N = 62) and encircled areas of preserved photopic function. In the other patients, AF rings either resembled those seen in RP or encircled an area of central atrophy. Ring radius was inversely related to the PERG P50 component in 4 of 18 cases with a detectable response. FMM showed that arcs of high density were associated with a gradient of sensitivity change. Conclusions Parafoveal rings of high density autofluorescence are a non-specific manifestation of retinal dysfunction that can occur in different retinal dystrophies. Electrophysiology remains essential for accurate diagnosis. The high correlation of autofluorescence with PERG, mfERG and FMM demonstrates that AF abnormalities have functional significance and may help identify suitable patients and retinal areas amenable to future therapeutic intervention.
Literature
1.
go back to reference Wing GL, Blanchard GC, Weiter JJ (1978) The topography and age relationship of lipofuscin concentration in the retinal pigment epithelium. Invest Ophthalmol Vis Sci 17:601–607PubMed Wing GL, Blanchard GC, Weiter JJ (1978) The topography and age relationship of lipofuscin concentration in the retinal pigment epithelium. Invest Ophthalmol Vis Sci 17:601–607PubMed
2.
go back to reference Feeney-Burns L, Eldred GE (1983) The fate of the phagosome: conversion to “Age Pigment” and impact in human retinal pigment epithelium. Trans Ophthal Soc UK 103:416–421PubMed Feeney-Burns L, Eldred GE (1983) The fate of the phagosome: conversion to “Age Pigment” and impact in human retinal pigment epithelium. Trans Ophthal Soc UK 103:416–421PubMed
3.
go back to reference Kennedy CJ, Rakoczy PE (1995) Constable IJ. Lipofuscin of the retinal pigment epithelium: a review. Eye 9:763–771PubMed Kennedy CJ, Rakoczy PE (1995) Constable IJ. Lipofuscin of the retinal pigment epithelium: a review. Eye 9:763–771PubMed
4.
go back to reference Delori FC, Goger DG, Dorey CK (2001) Age-related accumulation and spatial distribution of lipofuscin in RPE of normal subjects. Invest Ophthalmol Vis Sci. 42:1855–1866PubMed Delori FC, Goger DG, Dorey CK (2001) Age-related accumulation and spatial distribution of lipofuscin in RPE of normal subjects. Invest Ophthalmol Vis Sci. 42:1855–1866PubMed
5.
go back to reference von Rückmann A, Fitzke FW, Bird AC (1995) Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. Br J Ophthalmol 79:407–412CrossRef von Rückmann A, Fitzke FW, Bird AC (1995) Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. Br J Ophthalmol 79:407–412CrossRef
6.
go back to reference von Rückmann A, Fitzke FW, Bird AC (1999) Distribution of pigment epithelium autofluorescence in retinal disease state recorded in vivo and its change over time. Graefes Arch Clin Exp Ophthalmol 237:1–9CrossRef von Rückmann A, Fitzke FW, Bird AC (1999) Distribution of pigment epithelium autofluorescence in retinal disease state recorded in vivo and its change over time. Graefes Arch Clin Exp Ophthalmol 237:1–9CrossRef
7.
go back to reference Lois N, Holder GE, Fitzke FW, Plant C, Bird AC (1999) Intrafamilial variation of phenotype in Stargardt macular dystrophy-fundus flavimaculatus. Invest Ophthalmol Vis Sci 40:2668–2675PubMed Lois N, Holder GE, Fitzke FW, Plant C, Bird AC (1999) Intrafamilial variation of phenotype in Stargardt macular dystrophy-fundus flavimaculatus. Invest Ophthalmol Vis Sci 40:2668–2675PubMed
8.
go back to reference Lois N, Halfyard AS, Bird AC, Holder GE, Fitzke FW (2000) Quantitative evaluation of fundus autofluorescence imaged “in vivo” in eyes with retinal disease. Br J Ophthalmol 84:741–745PubMedCrossRef Lois N, Halfyard AS, Bird AC, Holder GE, Fitzke FW (2000) Quantitative evaluation of fundus autofluorescence imaged “in vivo” in eyes with retinal disease. Br J Ophthalmol 84:741–745PubMedCrossRef
9.
go back to reference Lois N, Holder GE, Bunce C, Fitzke FW, Bird AC (2001) Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol 119:359–369PubMed Lois N, Holder GE, Bunce C, Fitzke FW, Bird AC (2001) Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol 119:359–369PubMed
10.
go back to reference Kurz-Levin MM, Halfyard AS, Bunce C, Bird AC, Holder GE (2002) Clinical variations in assessment of bull’s-eye maculopathy. Arch Ophthalmol 120:567–575PubMed Kurz-Levin MM, Halfyard AS, Bunce C, Bird AC, Holder GE (2002) Clinical variations in assessment of bull’s-eye maculopathy. Arch Ophthalmol 120:567–575PubMed
11.
go back to reference Holz FG, Bellman C, Staudt S, Schütt F, Völcker HE (2001) Fundus autofluorescence and development of geographic atrophy in age-related macular degeneration. Invest Ophthalmol Vis Sci 42:1051–1056PubMed Holz FG, Bellman C, Staudt S, Schütt F, Völcker HE (2001) Fundus autofluorescence and development of geographic atrophy in age-related macular degeneration. Invest Ophthalmol Vis Sci 42:1051–1056PubMed
12.
go back to reference Holder GE, Robson AG, Hogg CR, Kurz-Levin M, Lois N, Bird AC (2003) Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy. Doc Ophthalmol 106:17–23PubMedCrossRef Holder GE, Robson AG, Hogg CR, Kurz-Levin M, Lois N, Bird AC (2003) Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy. Doc Ophthalmol 106:17–23PubMedCrossRef
13.
go back to reference Jarc-Vidmar M, Kraut A, Hawlina M (2003) Fundus autofluorescence imaging in Best’s vitelliform dystrophy. Klin Monatsbl Augenheilkd 220:861–867PubMedCrossRef Jarc-Vidmar M, Kraut A, Hawlina M (2003) Fundus autofluorescence imaging in Best’s vitelliform dystrophy. Klin Monatsbl Augenheilkd 220:861–867PubMedCrossRef
14.
go back to reference Zhou J, Jang YP, Kim SR, Sparrow JR (2006) Complement activation by photooxidation products of A2E, a lipofuscin constituent of the retinal pigment epithelium. Proc Natl Acad Sci USA 103:16182–16187PubMedCrossRef Zhou J, Jang YP, Kim SR, Sparrow JR (2006) Complement activation by photooxidation products of A2E, a lipofuscin constituent of the retinal pigment epithelium. Proc Natl Acad Sci USA 103:16182–16187PubMedCrossRef
15.
go back to reference Lorenz B, Wabbels B, Wegscheider E, Hamel CP, Drexler W, Preising MN (2004) Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65. Ophthalmology 111:1585–1594PubMedCrossRef Lorenz B, Wabbels B, Wegscheider E, Hamel CP, Drexler W, Preising MN (2004) Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65. Ophthalmology 111:1585–1594PubMedCrossRef
16.
go back to reference Henderson R, Lorenz B, Moore AT (2006) Clinical and molecular genetic aspects of Leber’s congenital amaurosis. In: Lorenz B (Eds) Essentials in ophthalmology. Springer-Verlag, Berlin, pp 133–155 Henderson R, Lorenz B, Moore AT (2006) Clinical and molecular genetic aspects of Leber’s congenital amaurosis. In: Lorenz B (Eds) Essentials in ophthalmology. Springer-Verlag, Berlin, pp 133–155
17.
go back to reference Robson AG, El-Amir A, Bailey C, Egan CA, Fitzke FW, Webster AR, Bird AC, Holder GE (2003) Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Invest Ophthalmol Vis Sci 44:3544–3550PubMedCrossRef Robson AG, El-Amir A, Bailey C, Egan CA, Fitzke FW, Webster AR, Bird AC, Holder GE (2003) Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Invest Ophthalmol Vis Sci 44:3544–3550PubMedCrossRef
18.
go back to reference Robson AG, Egan CA, Luong VA, Bird AC, Holder GE, Fitzke FW (2004) Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity. Invest Ophthalmol Vis Sci 45:4119–4125PubMedCrossRef Robson AG, Egan CA, Luong VA, Bird AC, Holder GE, Fitzke FW (2004) Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity. Invest Ophthalmol Vis Sci 45:4119–4125PubMedCrossRef
19.
go back to reference Robson AG, Egan C, Holder GE, Bird AC, Fitzke FW (2003) Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa. Adv Exp Med Biol 533:41–47PubMed Robson AG, Egan C, Holder GE, Bird AC, Fitzke FW (2003) Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa. Adv Exp Med Biol 533:41–47PubMed
20.
go back to reference Popovic P, Jarc-Vidmar M, Hawlina M (2005) Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa. Graefes Arch Clin Exp Ophthalmol 243:1018–1027PubMedCrossRef Popovic P, Jarc-Vidmar M, Hawlina M (2005) Abnormal fundus autofluorescence in relation to retinal function in patients with retinitis pigmentosa. Graefes Arch Clin Exp Ophthalmol 243:1018–1027PubMedCrossRef
21.
go back to reference Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC (2004) Fundus autofluorescence in patients with leber congenital amaurosis. Invest Ophthalmol Vis Sci 45:2747–2752PubMedCrossRef Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC (2004) Fundus autofluorescence in patients with leber congenital amaurosis. Invest Ophthalmol Vis Sci 45:2747–2752PubMedCrossRef
22.
go back to reference Tsang SH, Vaclavik V, Bird AC, Robson AG, Holder GE (2007) Novel phenotypic and genotypic findings in X-linked retinoschisis. Arch Ophthalmol 125:259–267PubMedCrossRef Tsang SH, Vaclavik V, Bird AC, Robson AG, Holder GE (2007) Novel phenotypic and genotypic findings in X-linked retinoschisis. Arch Ophthalmol 125:259–267PubMedCrossRef
23.
go back to reference Downes SM, Holder GE, Fitzke FW, Payne AM, Warren MJ, Bhattacharya SS, Bird AC (2001) Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. Arch Ophthalmol 119:96–105PubMed Downes SM, Holder GE, Fitzke FW, Payne AM, Warren MJ, Bhattacharya SS, Bird AC (2001) Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1. Arch Ophthalmol 119:96–105PubMed
24.
go back to reference Downes SM, Payne AM, Kelsell RE, Fitzke FW, Holder GE, Hunt DM, Moore AT, Bird AC (2001) Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. Arch Ophthalmol 119:1667–1673PubMed Downes SM, Payne AM, Kelsell RE, Fitzke FW, Holder GE, Hunt DM, Moore AT, Bird AC (2001) Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. Arch Ophthalmol 119:1667–1673PubMed
25.
go back to reference Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ (2005) Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families. Invest Ophthalmol Vis Sci 46:1891–1898PubMedCrossRef Ebenezer ND, Michaelides M, Jenkins SA, Audo I, Webster AR, Cheetham ME, Stockman A, Maher ER, Ainsworth JR, Yates JR, Bradshaw K, Holder GE, Moore AT, Hardcastle AJ (2005) Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families. Invest Ophthalmol Vis Sci 46:1891–1898PubMedCrossRef
26.
go back to reference Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW (2007) Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone-rod dystrophy. Br J Ophthalmol. Online First: 25 Oct 2007 Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW (2007) Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone-rod dystrophy. Br J Ophthalmol. Online First: 25 Oct 2007
27.
go back to reference Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT (2005) A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Br J Ophthalmol 89:198–206PubMedCrossRef Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT (2005) A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Br J Ophthalmol 89:198–206PubMedCrossRef
28.
go back to reference Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, Fitzke FW, Mollon JD, Moore AT (2005) A detailed phenotypic study of “cone dystrophy with supernormal rod ERG”. Br J Ophthalmol 89:332–339PubMedCrossRef Michaelides M, Holder GE, Webster AR, Hunt DM, Bird AC, Fitzke FW, Mollon JD, Moore AT (2005) A detailed phenotypic study of “cone dystrophy with supernormal rod ERG”. Br J Ophthalmol 89:332–339PubMedCrossRef
29.
go back to reference Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR (2006) Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause “cone dystrophy with supernormal rod electroretinogram” in humans. Am J Hum Genet 79:574–579PubMedCrossRef Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR (2006) Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause “cone dystrophy with supernormal rod electroretinogram” in humans. Am J Hum Genet 79:574–579PubMedCrossRef
30.
go back to reference Robson AG, Moreland JD, Pauleikhoff D, Morrissey T, Holder GE, Fitzke FW, Bird AC, van Kuijk FJ (2003) Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry. Vision Res 43:1765–1775PubMedCrossRef Robson AG, Moreland JD, Pauleikhoff D, Morrissey T, Holder GE, Fitzke FW, Bird AC, van Kuijk FJ (2003) Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry. Vision Res 43:1765–1775PubMedCrossRef
31.
go back to reference Marmor MF, Holder GE, Seeliger MW, Yamamoto S (2004) Standard for clinical electroretinography (2004 update) Doc Ophthalmol 108:107–114PubMedCrossRef Marmor MF, Holder GE, Seeliger MW, Yamamoto S (2004) Standard for clinical electroretinography (2004 update) Doc Ophthalmol 108:107–114PubMedCrossRef
32.
go back to reference Holder GE, Brigell MG, Hawlina M, Meigen T, Vaegan, Bach M (2007) ISCEV standard for clinical pattern electroretinography—2007 update. Doc Ophthalmol 114:111–116PubMedCrossRef Holder GE, Brigell MG, Hawlina M, Meigen T, Vaegan, Bach M (2007) ISCEV standard for clinical pattern electroretinography—2007 update. Doc Ophthalmol 114:111–116PubMedCrossRef
33.
go back to reference Marmor MF, Hood DC, Keating D, Kondo M, Seeliger MW, Miyake Y (2003) Guidelines for basic multifocal electroretinography (mfERG). Doc Ophthalmol 106:105–115PubMedCrossRef Marmor MF, Hood DC, Keating D, Kondo M, Seeliger MW, Miyake Y (2003) Guidelines for basic multifocal electroretinography (mfERG). Doc Ophthalmol 106:105–115PubMedCrossRef
34.
go back to reference Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE (2004) Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness. Invest Ophthalmol Vis Sci 45:2355–2360PubMedCrossRef Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE (2004) Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness. Invest Ophthalmol Vis Sci 45:2355–2360PubMedCrossRef
35.
go back to reference Chen JC, Fitzke FW, Pauleikhoff D, Bird AC (1992) Functional loss in age-related Bruch’s membrane change with choroidal perfusion defect. Invest Ophthalmol Vis Sci 33:334–340PubMed Chen JC, Fitzke FW, Pauleikhoff D, Bird AC (1992) Functional loss in age-related Bruch’s membrane change with choroidal perfusion defect. Invest Ophthalmol Vis Sci 33:334–340PubMed
36.
go back to reference Westcott MC, Garway-Heath DF, Fitzke FW, Kamal D, Hitchings RA (2002) Use of high spatial resolution perimetry to identify scotomata not apparent with conventional perimetry in the nasal field of glaucomatous subjects. Br J Ophthalmol 86:761–766PubMedCrossRef Westcott MC, Garway-Heath DF, Fitzke FW, Kamal D, Hitchings RA (2002) Use of high spatial resolution perimetry to identify scotomata not apparent with conventional perimetry in the nasal field of glaucomatous subjects. Br J Ophthalmol 86:761–766PubMedCrossRef
37.
go back to reference Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE (2006) Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Br J Ophthalmol 90:472–479PubMedCrossRef Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE (2006) Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Br J Ophthalmol 90:472–479PubMedCrossRef
38.
go back to reference Shu X, Black GC, Rice JM, Hart-Holden N, Jones A, O’Grady A, Ramsden S, Wright AF (2007) RPGR mutation analysis and disease: an update. Hum Mutat 28:322–328PubMedCrossRef Shu X, Black GC, Rice JM, Hart-Holden N, Jones A, O’Grady A, Ramsden S, Wright AF (2007) RPGR mutation analysis and disease: an update. Hum Mutat 28:322–328PubMedCrossRef
39.
go back to reference Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL (2007) Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations. Invest Ophthalmol Vis Sci 48:1298–1304PubMedCrossRef Sandberg MA, Rosner B, Weigel-DiFranco C, Dryja TP, Berson EL (2007) Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations. Invest Ophthalmol Vis Sci 48:1298–1304PubMedCrossRef
40.
go back to reference Katz ML, Drea CM, Eldred GE, Hess HH, Robison WG (1986) Influence of early photoreceptor degeneration on lipofuscin in the retinal pigment epithelium. Exp Eye Res 43:561–573PubMedCrossRef Katz ML, Drea CM, Eldred GE, Hess HH, Robison WG (1986) Influence of early photoreceptor degeneration on lipofuscin in the retinal pigment epithelium. Exp Eye Res 43:561–573PubMedCrossRef
41.
go back to reference Radu RA et al (2005): Reductions in serum vitamin A arrest accumulation of toxic retinal fluorophores: a potential therapy for treatment of lipofuscin-based retinal diseases. Invest Ophthalmol Vis Sci 46:4393–4401PubMedCrossRef Radu RA et al (2005): Reductions in serum vitamin A arrest accumulation of toxic retinal fluorophores: a potential therapy for treatment of lipofuscin-based retinal diseases. Invest Ophthalmol Vis Sci 46:4393–4401PubMedCrossRef
42.
go back to reference Katz ML, Redmond MT (2001) Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epithelium. Invest Ophthalmol Vis Sci 42:3023–3030PubMed Katz ML, Redmond MT (2001) Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epithelium. Invest Ophthalmol Vis Sci 42:3023–3030PubMed
43.
go back to reference Wabbels B, Demmler A, Paunescu K, Wegscheider E, Preising MN, Lorenz B (2006) Fundus autofluorescence in children and teenagers with hereditary retinal diseases. Graefes Arch Clin Exp Ophthalmol 244:36–45PubMedCrossRef Wabbels B, Demmler A, Paunescu K, Wegscheider E, Preising MN, Lorenz B (2006) Fundus autofluorescence in children and teenagers with hereditary retinal diseases. Graefes Arch Clin Exp Ophthalmol 244:36–45PubMedCrossRef
Metadata
Title
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update
Authors
Anthony G. Robson
Michel Michaelides
Zubin Saihan
Alan C. Bird
Andrew R. Webster
Anthony T. Moore
Fred W. Fitzke
Graham E. Holder
Publication date
01-03-2008
Publisher
Springer-Verlag
Published in
Documenta Ophthalmologica / Issue 2/2008
Print ISSN: 0012-4486
Electronic ISSN: 1573-2622
DOI
https://doi.org/10.1007/s10633-007-9087-4

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