Morgagnian cataract with congenital complete aniridia with congenital lenticular coloboma: A rare association

Complete congenital aniridia is a rare genetic ocular disease. We report a rare case of bilateral congenital complete aniridia in a 31-year-old male. He reported to the ophthalmology department when he experienced a significant decrease in vision in the right eye. On ocular examination, there was congenital complete aniridia with Morgagnian cataract with a congenital lenticular coloboma inferiorly in the right eye. The left eye also showed the presence of complete aniridia without any coloboma. Both eyes had mild corneal vascularisation with limbal stem cell deficiency. A diagnosis of congenital cataracts, megalocornea, limbal stem cell deficiency and inferior lenticular coloboma in the right eye was made. The patient underwent cataract surgery with aniridia intraocular lens in the right eye with a good visual outcome. Best-corrected visual acuity was improved to 20/40.

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Publication Details

Journal
Global Journal of Cataract Surgery and Research in Ophthalmology
Published
2025-09-20
DOI
https://doi.org/10.25259/gjcsro_14_2025
Primary Topic
Intraocular Surgery and Lenses
Type
article
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article

Morgagnian cataract with congenital complete aniridia with congenital lenticular coloboma: A rare association

Navreet Kaur, Rajwinder Kaur Bhattal
Global Journal of Cataract Surgery and Research in Ophthalmology
Intraocular Surgery and Lenses
article

Morgagnian cataract with congenital complete aniridia with congenital lenticular coloboma: A rare association

Navreet Kaur, Rajwinder Kaur Bhattal
article en

Abstract

Complete congenital aniridia is a rare genetic ocular disease. We report a rare case of bilateral congenital complete aniridia in a 31-year-old male. He reported to the ophthalmology department when he experienced a significant decrease in vision in the right eye. On ocular examination, there was congenital complete aniridia with Morgagnian cataract with a congenital lenticular coloboma inferiorly in the right eye. The left eye also showed the presence of complete aniridia without any coloboma. Both eyes had mild corneal vascularisation with limbal stem cell deficiency. A diagnosis of congenital cataracts, megalocornea, limbal stem cell deficiency and inferior lenticular coloboma in the right eye was made. The patient underwent cataract surgery with aniridia intraocular lens in the right eye with a good visual outcome. Best-corrected visual acuity was improved to 20/40.

Global Journal of Cataract Surgery and Research in OphthalmologyVol. 4
Adesh University (IN)
Openalex Percentile: Top 62%
Intraocular Surgery and Lenses
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Morgagnian cataract with congenital complete aniridia with congenital lenticular coloboma: A rare association — Navreet Kaur, Rajwinder Kaur Bhattal · Global Journal of Cataract Surgery and Research in Ophthalmology (2025) | TGRS Research Map | TGRS