Analysis of retinal flecks in fundus flavimaculatus using high-definition spectral-domain optical coherence tomography

American Journal of Ophthalmology

Volumn 150, Issue 3, 2010, Pages 330-337

  Voigt, Monika ^a   Querques, Giuseppe ^a   Atmani, Karim ^a   Leveziel, Nicolas ^a   Massamba, Nathalie ^a   Puche, Nathalie ^a   Bouzitou Mfoumou, Rislie ^a   Souied, Eric H ^a  

^a UNIVERSITÉ PARIS EST CRÉTEIL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOFLUORESCENCE IMAGING; BRUCH MEMBRANE; CLINICAL ARTICLE; DRUSEN; EYE DISEASE; EYE FUNDUS FLAVIMACULATUS; FEMALE; HUMAN; MALE; MORPHOLOGY; OPTICAL COHERENCE TOMOGRAPHY; PHOTORECEPTOR OUTER SEGMENT; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA; SCANNING LASER OPHTHALMOSCOPE;

ADULT; AGED; FEMALE; FLUORESCEIN ANGIOGRAPHY; FUNDUS OCULI; HUMANS; MALE; MIDDLE AGED; OPHTHALMOSCOPY; PHOTORECEPTOR CELLS, VERTEBRATE; RETINAL DEGENERATION; RETINAL PIGMENT EPITHELIUM; TOMOGRAPHY, OPTICAL COHERENCE; VISUAL ACUITY; YOUNG ADULT;

EID: 77956059871     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajo.2010.04.001     Document Type: Article

References (27)

1. K. Stargardt Ueber familiare progressive Degeneration in der Makulagegend des Auges Albrecht V Graefes Arch Ophthalmol 71 1909 534 550
2. G.W. Cibis, M. Morey, and D.J. Karris Dominantly inherited macular dystrophy with flecks (Stargardt) Arch Ophthalmol 98 10 1980 1785
3. S. Merin, and J. Landau Abnormal findings in relatives of patients with juvenile hereditary macular degeneration (Stargardt's disease) Ophthalmologica 161 1 1970 1 10
4. A. Franceschetti, and J. Francois Fundus flavimaculatus Arch Ophthalmol 25 6 1965 505
5. R. Allikmets, N. Singh, and H. Sun A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy Nat Genet 15 3 1997 236 246
6. F.P. Cremers, D.J. van de Pol, and M. van Driel Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR Hum Mol Genet 7 3 1998 355 362
7. J.M. Rozet, S. Gerber, and E. Souied Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies Eur J Hum Genet 6 3 1998 291 295
8. A.V. Cideciyan, T.S. Aleman, and M. Swider Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence Hum Mol Genet 13 5 2004 525 534
9. T.M. Aaberg Stargardt's disease and fundus flavimaculatus: evaluation of morphologic progression and intrafamilial co-existence Trans Am Ophtalmol Soc 84 1986 453 487
10. N. Lois, G.E. Holder, C. Bunce, F.W. Fitzke, and A.C. Bird Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus Arch Ophthalmol 119 3 2001 359 369
11. Y. Rotenstreich, G.A. Fishman, and R.J. Anderson Visual acuity loss and clinical observations in a large series of patients with Stargardt disease Ophthalmology 110 6 2003 1151 1158
12. C. Gerth, M. Andrassi-Darida, M. Bock, M.N. Preising, B.H. Weber, and B. Lorenz Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlation Graefes Arch Clin Exp Ophthalmol 240 8 2002 628 638
13. B.J. Klevering, M. van Driel, D.J. van de Pol, A.J. Pinckers, F.P. Cremers, and C.B. Hoyng Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene Br J Ophthalmol 83 8 1999 914 918
14. F.G. Holz Autofluorescence imaging of the macula Ophthalmologe 98 1 2001 10 18
15. A. Von Ruckmann, F.W. Fitzke, and A.C. Bird In vivo autofluorescence in macular dystrophies Arch Ophthalmol 115 5 1997 609 615
16. E. Souied, J. Kaplan, and G. Coscas Macular dystrophies J Fr Ophtalmol 26 7 2003 743 762
17. G. Querques, N. Leveziel, N. Benhamou, M. Voigt, G. Soubrane, and E.H. Souied Analysis of retinal flecks in fundus flavimaculatus using optical coherence tomography Br J Ophthalmol 90 9 2006 1157 1162
18. R. Zawadzki, S. Jones, and S. Olivier Adaptive-optics optical coherence tomography for high-resolution and high-speed 3D retinal in-vivo imaging Opt Express 13 2005 8532 8546
19. M. Pircher, E. Gotzinger, and O. Findl Human macula investigated in vivo with polarization-sensitive optical coherence tomography Invest Ophthalmol Vis Sci 47 12 2006 5487 5494
20. W. Drexler Cellular and functional optical coherence tomography of the human retina: the Cogan lecture 1 Invest Ophthalmol Vis Sci 48 12 2007 5339 5351
21. S. Michels, M. Pircher, and W. Geitzenauer Value of polarization sensitive optical coherence tomography in diseases affecting the retinal pigment epithelium Br J Ophthalmol 92 2 2008 204 209
22. M. Fleckenstein, P. Charbel Issa, and H.M. Helb High-resolution spectral domain-OCT imaging in geographic atrophy associated with age-related macular degeneration Invest Ophthalmol Vis Sci 49 9 2008 4137 4144
23. C. Gerth, R.J. Zawadzki, S.S. Choi, J.L. Keltner, S.S. Park, and J.S. Werner Visualization of lipofuscin accumulation in Stargardt macular dystrophy by high-resolution Fourier-domain optical coherence tomography Arch Ophthalmol 125 4 2007 575
24. C. Bellmann, F.G. Holz, and O. Schapp Topography of fundus antofluorescence with a new confocal scanning laser ophthalmoscope Ophthalmologe 94 6 1997 385 391
25. E. Ergun, B. Hermann, and M. Wirtitsch Assessment of central visual function in Stargardt's disease/fundus flavimaculatus with ultrahigh-resolution optical coherence tomography Invest Ophthalmol Vis Sci 46 1 2005 310 316
26. G. Querques, R. Prato, and C. Iaculli Correlation of visual function impairment and OCT findings in patients with Stargardt disease and fundus flavimaculatus Eur J Ophthalmol 18 2 2008 239 247
27. N.L. Gomes, V.C. Greenstein, and J.N. Carlson A comparison of fundus autofluorescence and retinal structure in patients with Stargardt disease Invest Ophthalmol Vis Sci 50 8 2009 3953 3959