Circumferential iris transillumination defects in exfoliation syndrome

Journal of Glaucoma

Volumn 22, Issue 7, 2013, Pages 555-558

  Fingert, John H ^a   Burden, James H ^a   Wang, Kai ^b   Kwon, Young H ^a   Alward, Wallace L M ^a   Anderson, Michael G ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

Diagnostic sign; Exfoliation syndrome; iris transillumination defects

Indexed keywords

IMMUNOREACTIVE INSULIN;

ARTICLE; CIRCUMFERENTIAL IRIS TRANSILLUMINATION DEFECT; CLINICAL ARTICLE; COMPUTER PROGRAM; CONTROLLED STUDY; DIAGNOSTIC IMAGING; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; EARLY DIAGNOSIS; EYE COLOR; HUMAN; INFRARED PHOTOGRAPHY; INFRARED RADIATION; INFRARED VIDEOGRAPHY; IRIS DISEASE; OPEN ANGLE GLAUCOMA; OPHTHALMOLOGICAL DIAGNOSTIC DEVICE; PIGMENT DISPERSION SYNDROME; PRIORITY JOURNAL; PSEUDOEXFOLIATION; VIDEORECORDING; VIDEOTAPE;

CASE-CONTROL STUDIES; EXFOLIATION SYNDROME; GLAUCOMA, OPEN-ANGLE; GONIOSCOPY; HUMANS; INFRARED RAYS; INTRAOCULAR PRESSURE; IRIS DISEASES; OCULAR HYPERTENSION; PROSPECTIVE STUDIES; VIDEO RECORDING;

EID: 84883559052     PISSN: 10570829     EISSN: 1536481X     Source Type: Journal    
DOI: 10.1097/IJG.0b013e318255da16     Document Type: Article

References (20)

1. Ritch R. Exfoliation syndrome: Beyond glaucoma. Arch Ophthalmol. 2008;126:859-861
2. Ritch R, Schlötzer-Schrehardt U. Exfoliation syndrome. Surv Ophthalmol. 2001;45:265-315
3. Thorleifsson G, Magnusson KP, Sulem P, et al. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007;317:1397-1400
4. Fingert JH, Alward WL, Kwon YH, et al. LOXL1 mutations are associated with exfoliation syndrome in patients from the Midwestern United States. Am J Ophthalmol. 2007;144: 974-975
5. Yang X, Zabriskie NA, Hau VS, et al. Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort. Cell Cycle. 2008;7:521-524
6. Challa P, Schmidt S, Liu Y, et al. Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma. Mol Vis. 2008;14:146-149
7. Aragon-Martin JA, Ritch R, Liebmann J, et al. Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma. Mol Vis. 2008;14:533-541
8. Fan BJ, Pasquale L, Grosskreutz CL, et al. DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity. BMC Med Genet. 2008;9:5
9. Pasutto F, Krumbiegel M, Mardin CY, et al. Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Invest Ophthalmol Vis Sci. 2008;49:1459-1463
10. Hewitt AW, Sharma S, Burdon KP, et al. Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people. Hum Mol Genet. 2008;17:710-716
11. Ramprasad VL, George R, Soumittra N, et al. Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India. Mol Vis. 2008;14:318-322
12. Hayashi H, Gotoh N, Ueda Y, et al. Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population. Am J Ophthalmol. 2008;145:582-585
13. Ozaki M, Lee KY, Vithana EN, et al. Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese. Invest Ophthalmol Vis Sci. 2008;49:3976-3980
14. Abu-Amero KK, Osman EA, Dewedar AS, et al. Analysis of LOXL1 polymorphisms in a Saudi Arabian population with pseudoexfoliation glaucoma. Mol Vis. 2010;16:2805-2810
15. Williams SE, Whigham BT, Liu Y, et al. Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Mol Vis. 2010;16:705-712
16. Ferrell G, Lu M, Stoddard P, et al. A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes. Reprod Sci. 2009;16:438-446
17. Fan BJ, Pasquale LR, Rhee D, et al. LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Invest Ophthalmol Vis Sci. 2011;52: 2372-2378
18. Trantow CM, Mao M, Petersen GE, et al. Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome. Invest Ophthalmol Vis Sci. 2009;50:1205-1214
19. Alward WL, Fingert JH, Coote MA, et al. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A). N Engl J Med. 1998;338:1022-1027
20. Alward WL, Munden PM, Verdick RE, et al. Use of infrared videography to detect and record iris transillumination defects. Arch Ophthalmol. 1990;108:748-750