Bilateral morganian cataract in patient with congenital aniridia - case report

Authors

DOI:

https://doi.org/10.11606/issn.1679-9836.v99i5p519-522

Keywords:

Aniridia, Cataract, Cataract/genetics, Surgery.

Abstract

Decreased vision due to significant opacity of media is common in aniridia, but there are few reports of combined surgery in this condition. Cataract surgery with polymethylmethacrylate intraocular lens implantation remains a challenge for surgeons due to the greater weight of this material and the zonular dialysis presented by these patients. The present study aims to report a case of aniridia in a young patient with hypermature cataract.

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Author Biographies

  • Lara Picanço Scarpini, Hospital Santa Casa de Misericórdia de Vitória

    Trabalho realizado no Serviço de Oftalmologia da Santa Casa de Misericórdia de Vitória, Vitória, ES, Brasil
    Residente do 3º ano de Oftalmologia do Hospital da Santa Casa de Misericórdia de Vitória.

  • Lucas Siegle Valbon, Hospital Santa Casa de Misericórdia de Vitória

    Trabalho realizado no Serviço de Oftalmologia da Santa Casa de Misericórdia de Vitória, Vitória, ES, Brasil
    Residente do 3º ano de Oftalmologia do Hospital da Santa Casa de Misericórdia de Vitória.

  • Rafael Fernandes Silva, Hospital dos Servidores do Estado do Rio de Janeiro

    Trabalho realizado no Serviço de Oftalmologia da Santa Casa de Misericórdia de Vitória, Vitória, ES, Brasil
    Fellowship em retina clínica no Hospital dos Servidores do Estado do Rio de Janeiro.

  • Bruno de Freitas Valbon, Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória

    Professor Adjunto da Disciplina de Oftalmologia da Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória.

References

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Published

2020-12-10

Issue

Section

Relato de Caso/Case Report

How to Cite

Scarpini, L. P., Valbon, L. S., Silva, R. F., & Valbon, B. de F. (2020). Bilateral morganian cataract in patient with congenital aniridia - case report. Revista De Medicina, 99(5), 519-522. https://doi.org/10.11606/issn.1679-9836.v99i5p519-522