Bilateral Congenital Aniridia with Bilateral Sensorineural Hearing Loss

In this case report we aimed to report a 9 years old child who has bilateral congenital aniridia, cataract, high intraocular pressure, strabismus and sensorineural hearing loss

📌 3 Key Takeaways

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Objective & Hypothesis:Total or partial defect of iris is called anirida.

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Key Findings & Data:It may be congenital or may occur secondary to trauma.

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Conclusion & Impact:In this case report we aimed to report a 9 years old child who has bilateral congenital aniridia, cataract, high intraocular pressure, strabismus and sensorineural hearing loss

🔬Design:Research Article

📍Scope:Comprehensive Sample

⚙️Variables:Domain Parameters

Abstract

Total or partial defect of iris is called anirida. It may be congenital or may occur secondary to trauma. Bilateral congenital aniridia is a rare clinical condition. Its inheritance is usually autosomal dominant but sporadic cases are also been reported. In this case report we aimed to report a 9 years old child who has bilateral congenital aniridia, cataract, high intraocular pressure, strabismus and sensorineural hearing loss

Özet

Aniridi, irisin total veya parsiyel defektidir. Konjenital veya travmaya sekonder ortaya çıkabilir. Konjenital bilateral aniridi nadir görülen, genellikle otozomal dominant kalıtım gösteren ancak sporadik de görülebilen klinik bir durumdur. Bu yazıda, 9 yaşında görme azlığı ile kliniğimize başvuran, bilateral konjenital aniridi, katarakt, yüksek göz içi basıncı, şaşılık ve sensörinoral işitme kaybı olan olguyu sunmayı amaçladık

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Cite This Article

DOĞAN, M., ÖZCAN, S., POLAT, O., DUMAN, R., YAVAŞ, G. F., İNAN, Ü. (2016). Bilateral Congenital Aniridia with Bilateral Sensorineural Hearing Loss. Glokom Katarakt, Cilt: 11 - Sayı: 2, 133–135. https://ajindex.com/articles/197455

References (13)

Lawan A. Congenital eye and adnexial anomalies in Kano, a five year review. Niger J Med 2008;17:37-9.
Bodunde OT, Ajibode HA. Congenital eye diseases at Olabisi Ona- banjo University Teaching Hospital, Sagamu, Nigeria. Niger J Med 2006;15:291-4.
Nelson LB, Spaeth GL, Nowinski TS et al. Aniridia a review. Surv Oph- thalmol 1984;28:621-42.
Eden U, Iggman D, Ruse R et al. Epidemiology of aniridia in Sweden and Norway. Acta Ophthalmol 2008;86:727-9.
Baulmann DC, Ohlmann A, Flugel-Koch C et al. Pax6 heterozygous eyes show defects in chamber angle differentiation that are associated with a wide spectrum of other anterior eye segment abnormalities. Mech Dev 2002;118:3-17.
Traboulsi EI, Ellison J, Sears J et al. Aniridia with preserved visual func- tion: a report of four cases with no mutations in Pax6. Am J Ophthalmol 2008;145:760-4.
Lyons LA, Martha A, Mintz-Hittner HA et al. Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chro- mosome 11p13. Genomics 1992;13:925-30.
Whitson JT, Liang C, Godfrey DG et al. Central corneal thickness in pati- ents with congenital aniridia. Eye Contact Lens 2005;31:221-4.
McCulley TJ, Mayer K, Dahr SS et al. Aniridia and optic nerve hypopla- sia. Eye (Lond) 2005;19:762-4.
Dahl E, Koseki H, Balling R. Pax genes and organogenesis. Bioessays 1997;19:755-65
Grant WM, Walton DS. Progressive changes in the angle in congeni- tal aniridia, with development of glaucoma. Trans Am Ophthalmol Soc 1974;72:207-28.
Okudan S, Gündüz K, Özkağnıcı A, Öncel İ. Bilateral Aniridili Üç Olgu. Turkiye Klinikleri Journal of Ophthalmology, 1992,1:242-44.
Brandt JD, Casuso LA, Budenz DL. Markedly increased central corneal thickness: an unrecognized finding in congenital aniridia. Am J Ophthal- mol 2004;137:348-50.