Outer retina analysis by optical coherence tomography in cone-rod dystrophy patients

Retina

Volumn 33, Issue 9, 2013, Pages 1877-1880

  Lima, Luiz H ^a,b   Sallum, Juliana M F ^b   Spaide, Richard F ^a  

^a VITREOUS RETINA MACULA CONSULTANTS OF NEW YORK   (United States)

^b FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

cone rod dystrophy; optical coherence tomography; photoreceptors; retinal pigment epithelium

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; DARK ADAPTATION; ELECTRORETINOGRAPHY; FEMALE; HUMAN; MALE; PHOTOPIC VISION; PIGMENT EPITHELIUM; RETINA CONE ROD DYSTROPHY; RETINA DYSTROPHY; RETINA EXAMINATION; RETINA MACULA CYSTOID EDEMA; RETINA MACULOPATHY; RETROSPECTIVE STUDY; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY; VISUAL ACUITY;

EID: 84885020997     PISSN: 0275004X     EISSN: 15392864     Source Type: Journal    
DOI: 10.1097/IAE.0b013e31829234e6     Document Type: Article

References (17)

1. Michaelides M, Hunt DM, Moore AT. The cone dysfunction syndromes. Br J Ophthalmol 2004;88:291-297. (Pubitemid 38142106)
2. Simunovic MP, Moore AT. The cone dystrophies. Eye (Lond) 1998;12:553-565. (Pubitemid 28356665)
3. Hamel CP. Cone rod dystrophies. Orphanet J Rare Dis 2007;2: 1-7.
4. Berger W, Kloeckener-Gruissem B, Neidhardt J. The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res 2010;29:335-375.
5. Michaelides M, Hardcastle AJ, Hunt DM, Moore AT. Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis. Surv Ophthalmol 2006; 51:232-258.
6. Buch PK, Mihelec M, Cottrill P, et al. Dominant cone-rod dystrophy: a mouse model generated by gene targeting of the GCAP1/Guca1a gene. PLoS One 2011;6:e18089.
7. Lhériteau E, Libeau L, Stieger K, et al. The RPGRIP1-deficient dog, a promising canine model for gene therapy. Mol Vis 2009;15:349-361.
8. Conley S, Nour M, Fliesler SJ, Naash MI. Late-onset cone photoreceptor degeneration induced by R172W mutation in rds and partial rescue by gene supplementation. Invest Ophthalmol Vis Sci 2007;48:5397-5407. (Pubitemid 351260838)
9. Goldstein O, Mezey JG, Boyko AR, et al. An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9. Mol Vis 2010;16:1549-1569.
10. Parry DA, Toomes C, Bida L, et al. Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice. Am J Hum Genet 2009;84:683-691.
11. Spaide RF. Questioning optical coherence tomography. Ophthalmology 2012;19:2203-2204.
12. Hood DC, Zhang X, Ramachandran R, et al. The inner segment/outer segment border seen on optical coherence tomography is less intense in patients with diminished cone function. Invest Ophthalmol Vis Sci 2011;52:9703-9709.
13. Spaide RF, Curcio CA. Anatomical correlates to the bands seen in the outer retina by optical coherence tomography. Retina 2011;31:1609-1619.
14. Demirci FY, Gupta N, Radak AL, et al. Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15. Am J Ophthalmol 2005;139: 386-388. (Pubitemid 40288303)
15. Fujiwara T, Imamura Y, Margolis R, et al. Enhanced depth imaging optical coherence tomography of the choroid in highly myopic eyes. Am J Ophthalmol 2009;148:445-450.
16. Nishida Y, Fujiwara T, Imamura Y, et al. Choroidal thickness and visual acuity in highly myopic eyes. Retina 2012;32:1229-1236.
17. Switzer DW Jr, Mendonça LS, Saito M, et al. Segregation of ophthalmoscopic characteristics according to choroidal thickness in patients with early age-related macular degeneration. Retina 2012;32:1265-1271.