Peters’s anomaly. A clinical case presentation
Keywords:
congenital defect, central leucoma, treatmentAbstract
It described a case with anomaly of Peters, congenital defect of the cornea that appears of way generally sporadic and of etiology even uncertain. It does reference to his forms of presentation and to the possible treatments being the darkest prognosis when it accompanies of systemic manifestations. It explained how the diagnostic was reached. It is essentially clinical, letting some final considerations.
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References
1. Rezende RA, Uchoa UB, Uchoa R, Rapuano CJ, Laibson PR, Cohen EJ. Congenital corneal opacities in a cornea referral practice. Cornea. 2004; 23(6):565-70.
2. Harissi-Dagher M, Colby K. Anterior segment dysgenesis: Peters’ anomaly and sclerocornea. Int Ophthalmol Clin. 2008; 48(2):35-42. Review.
3. Bahn CF, Falls HF, Varley GA, Meyer RF, Edelhauser HF, Bourne WM. Classification of corneal endothelial disorders based on neural crest origin. Ophthalmology.1984; 91(6):558-63.
4. Maillette de Buy Wenniger-Prick LJ, Hennekam RC. The Peters’ plus syndrome: areview. Ann Genet. 2002; 45(2):97-103. Review.
5. Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA. Peters’ anomaly. The spectrum of associated ocular and systemic malfor-mations. Ophthalmic Paediatr Genet. 1992; 13(2):137-43.
6. Bhandari R, Ferri S, Whittaker B, Liu M, Lazzaro DR. Peters anomaly: review of the literature. Cornea. 2011; 30:939–44.
7. Eguía Martínez Frank et al. Manual de diagnóstico y tratamiento en Oftalmología. La Habana: ECIMED, 2009.
8. KanskyJJ.Oftalmología clínica VIed. España: Ed Elsevier,2006.
9. Ozeki H, Shirai S, Nozaki M, Sakurai E, Mizuno S, Ashikari M, Matsunaga N, Ogura Y: Ocular and systemic features of Peters anomaly. Graefes Arch Clin Exp Opthalmol 2000, 235:833-839.
10. MajanderAS,Lindahi PM,Vasara LK,Krootilla K.Anterior segment optical coherence tomography in congenital corneal opacities. Ophtalmology 2012; 119:2450-2457.
11. Nishide T,Nakanishi M,Hayakawa N,et al.Cataract surgery for tilted lens in Peters anomaly type 2.Case rep. Ophthalmol 2013;4:134- 7.
12. Lorry EA, Porco TC, Naseri A.Cost analysis of virtual – reality phacoemulsification in ophthalmology training programs. J Cataract Refract Surgery 2013; 39 1616- 7.
13. Nischal KK. A new appoach to the clasication of neonatal corneal opacities. Curr Opin Ophthalmol. 2012; 23:344-54.
14. Zaidman GW, Flanagan JK, Furey CC. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. Am J Ophthalmol. 2007; 144:104–108.
15. Lowe MT, Keane MC, Coster DJ, Williams KA. The outcome of corneal transplantation in infants, children, and adolescents. Ophthalmology. 2011; 118: 492–497.
16. Martin Al,Hodge C, Lowlessal, Roberts T, Hughes P, Sutton G. Femtosecond laser cataract surgery: Challengin cases. Curr Opin Ophthalmol. 2014; 25:71 -80.
2. Harissi-Dagher M, Colby K. Anterior segment dysgenesis: Peters’ anomaly and sclerocornea. Int Ophthalmol Clin. 2008; 48(2):35-42. Review.
3. Bahn CF, Falls HF, Varley GA, Meyer RF, Edelhauser HF, Bourne WM. Classification of corneal endothelial disorders based on neural crest origin. Ophthalmology.1984; 91(6):558-63.
4. Maillette de Buy Wenniger-Prick LJ, Hennekam RC. The Peters’ plus syndrome: areview. Ann Genet. 2002; 45(2):97-103. Review.
5. Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA. Peters’ anomaly. The spectrum of associated ocular and systemic malfor-mations. Ophthalmic Paediatr Genet. 1992; 13(2):137-43.
6. Bhandari R, Ferri S, Whittaker B, Liu M, Lazzaro DR. Peters anomaly: review of the literature. Cornea. 2011; 30:939–44.
7. Eguía Martínez Frank et al. Manual de diagnóstico y tratamiento en Oftalmología. La Habana: ECIMED, 2009.
8. KanskyJJ.Oftalmología clínica VIed. España: Ed Elsevier,2006.
9. Ozeki H, Shirai S, Nozaki M, Sakurai E, Mizuno S, Ashikari M, Matsunaga N, Ogura Y: Ocular and systemic features of Peters anomaly. Graefes Arch Clin Exp Opthalmol 2000, 235:833-839.
10. MajanderAS,Lindahi PM,Vasara LK,Krootilla K.Anterior segment optical coherence tomography in congenital corneal opacities. Ophtalmology 2012; 119:2450-2457.
11. Nishide T,Nakanishi M,Hayakawa N,et al.Cataract surgery for tilted lens in Peters anomaly type 2.Case rep. Ophthalmol 2013;4:134- 7.
12. Lorry EA, Porco TC, Naseri A.Cost analysis of virtual – reality phacoemulsification in ophthalmology training programs. J Cataract Refract Surgery 2013; 39 1616- 7.
13. Nischal KK. A new appoach to the clasication of neonatal corneal opacities. Curr Opin Ophthalmol. 2012; 23:344-54.
14. Zaidman GW, Flanagan JK, Furey CC. Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I. Am J Ophthalmol. 2007; 144:104–108.
15. Lowe MT, Keane MC, Coster DJ, Williams KA. The outcome of corneal transplantation in infants, children, and adolescents. Ophthalmology. 2011; 118: 492–497.
16. Martin Al,Hodge C, Lowlessal, Roberts T, Hughes P, Sutton G. Femtosecond laser cataract surgery: Challengin cases. Curr Opin Ophthalmol. 2014; 25:71 -80.
How to Cite
1.
Rodríguez Cambas A, Matos López U, Francisco Domingos M, Tirado Soler M. Peters’s anomaly. A clinical case presentation. Rev Inf Cient [Internet]. 2018 Mar. 2 [cited 2025 Apr. 3];97(2):362-8. Available from: https://revinfcientifica.sld.cu/index.php/ric/article/view/1854
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Case Reports
