Congenital Aniridia: Long-term Clinical Course, Visual Outcome, and Prognostic Factors
1
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Purpose: To describe the clinical course of congenital aniridia and to evaluate prognostic factors for visual outcomeafter long-term follow-up. Methods: The medical records of 120 eyes from 60 patients with congenital aniridia were retrospectively reviewed. The prevalence and clinical course of ophthalmic characteristics, systemic disease, refractive errors,and visual acuity were assessed. Prognostic factors for final visual outcomes were analyzed. Results: Aniridic keratopathy developed in 82 (69%) of 119 eyes. Macular hypoplasia was observed in 70 eyesof 35 patients (91%). Cataract was observed in 63 of 120 eyes (53%). Nystagmus was present in 41 patients(68% of 60 patients) at the initial visit but decreased in five patients (8% of 60 patients). Ocular hypertensionwas detected in 19 eyes (20% of 93 eyes), six (32% of 19 eyes) of which developed secondarily after cataractsurgery. The mean changes in spherical equivalent and astigmatism during the follow-up period were -1.10and 1.53 diopter, respectively. The mean final visual acuity was 1.028 logarithm of minimal angle of resolution. Nystagmus and ocular hypertension were identified as prognostic factors for poor visual outcome. Conclusions: Identification of nystagmus and ocular hypertension was important to predict final visual outcome. Based on the high rate of secondary ocular hypertension after cataract surgery, careful management is needed.
Abstract
Purpose: To describe the clinical course of congenital aniridia and to evaluate prognostic factors for visual outcomeafter long-term follow-up. Methods: The medical records of 120 eyes from 60 patients with congenital aniridia were retrospectively reviewed. The prevalence and clinical course of ophthalmic characteristics, systemic disease, refractive errors,and visual acuity were assessed. Prognostic factors for final visual outcomes were analyzed. Results: Aniridic keratopathy developed in 82 (69%) of 119 eyes. Macular hypoplasia was observed in 70 eyesof 35 patients (91%). Cataract was observed in 63 of 120 eyes (53%). Nystagmus was present in 41 patients(68% of 60 patients) at the initial visit but decreased in five patients (8% of 60 patients). Ocular hypertensionwas detected in 19 eyes (20% of 93 eyes), six (32% of 19 eyes) of which developed secondarily after cataractsurgery. The mean changes in spherical equivalent and astigmatism during the follow-up period were -1.10and 1.53 diopter, respectively. The mean final visual acuity was 1.028 logarithm of minimal angle of resolution. Nystagmus and ocular hypertension were identified as prognostic factors for poor visual outcome. Conclusions: Identification of nystagmus and ocular hypertension was important to predict final visual outcome. Based on the high rate of secondary ocular hypertension after cataract surgery, careful management is needed.
참고문헌 (23)
- Ton CC, "Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region", Cell, 67, pp.1059~1074 (1991)
- Glaser T, "Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene", Nat Genet, 2, pp.232~239 (1992)
- Churchill A, "Genetics of aniridia and anterior segment dysgenesis", Br J Ophthalmol, 80, pp.669~673 (1996)
- Nelson LB, "Aniridia: a review", Surv Ophthalmol, 28, pp.621~642 (1984)
- Eden U, "Epidemiology of aniridia in Sweden and Norway", Acta Ophthalmol, 86, pp.727~729 (2008)
- Eden U, "Aniridia among children and teenagers in Sweden and Norway", Acta Ophthalmol, 86, pp.730~734 (2008)
- Mannens M, "Autosomal dominant aniridia linked to the chromosome 11p13markers catalase and D11S151 in a large Dutch family", Cytogenet Cell Genet, 52, pp.32~36 (1989)
- Neuhann IM, "Cataract surgery and aniridia", Curr Opin Ophthalmol, 21, pp.60~64 (2010)
- Lee H, "Aniridia: current pathology and management", Acta Ophthalmol, 86, pp.708~715 (2008)
- De la Paz MF, "Long-term visual prognosis of corneal and ocular surface surgery in patients with congenital aniridia", Acta Ophthalmol, 86, pp.735~740 (2008)
- Lee H, "Complications and visual prognosis in children with aniridia", J Pediatr Ophthalmol Strabismus, 47, pp.205~210 (2010)
- Schulze-Bonsel K, "Visual acuities “hand motion” and “counting fingers” can be quantified with the freiburg visual acuity test", Invest Ophthalmol Vis Sci, 47, pp.1236~1240 (2006)
- Nishina S, "PAX6 expression in the developing human eye", Br J Ophthalmol, 83, pp.723~727 (1999)
- Azuma N, "PAX6 missense mutation in isolated foveal hypoplasia", Nat Genet, 13, pp.141~142 (1996)
- McCulley TJ, "Aniridia and optic nerve hypoplasia", Eye, 19, pp.762~764 (2005)
- Holmstrom G, "Optical coherence tomography is helpful in the diagnosis of foveal hypoplasia", Acta Ophthalmol, 88, pp.439~442 (2010)
- Grove JH, "A family study of aniridia", Arch Ophthalmol, 65, pp.81~94 (1961)
- Elsas FJ, "Familial aniridia with preserved ocular function", Am J Ophthalmol, 83, pp.718~724 (1977)
- Sonoda S, "A novel PAX6 gene mutation (P118R) in a family with congenital nystagmus associated with a variant form of aniridia", Graefes Arch Clin Exp Ophthalmol, 238, pp.552~558 (2000)
- Grant WM, "Progressive changes in the angle in congenital aniridia, with development of glaucoma", Trans Am Ophthalmol Soc, 72, pp.207~228 (1974)
- 박신혜, "Clinical Features of Korean Patients with Congenital Aniridia", Korean Journal of Ophthalmology, 24(5), pp.291~296 (2010), 대한안과학회
- Taylor RH, "The epidemiology of pediatric glaucoma: the Toronto experience", J AAPOS, 3, pp.308~315 (1999)
- Eden U, "Corneal involvement in congenital aniridia", Cornea, 29, pp.1096~1102 (2010)
