Journals / Acta Oncologica Turcica / 2012 / Cilt: 45 Sayı: 1

Congenital Heterochromia: A Case Report

Kongenital Heterokromi: Olgu Sunumu

Pages
18–20
Publication Date
2012-04-01
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this study, we aimed to present a patient with congenital heterochromia.

📌 3 Key Takeaways

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Objective & Hypothesis:Heterochromia iridis is a rare condition that often defined as eye color difference between the two eyes.
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Key Findings & Data:It can be congenital or either a component of a syndromic disease or a result of an eye disease.
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Conclusion & Impact:In this study, we aimed to present a patient with congenital heterochromia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Heterokromi · konjenital · iris

Abstract

Heterochromia iridis is a rare condition that often defined as eye color difference between the two eyes. It can be congenital or either a component of a syndromic disease or a result of an eye disease. In this study, we aimed to present a patient with congenital heterochromia.

Özet

Heterokromi iridis genellikle her iki göz rengi arasında fark olmasıyla tanımlanan nadir görülen bir durumdur. Sendromik bir hastalığın komponenti, bir göz hastalığının sonucu veya konjenital olarak ortaya çıkabilmektedir. Biz bu çalışmada konjenital heterokromili bir hastayı sunmayı amaçladık.

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Cite This Article

DUMAN, R., KARSLIOĞLU, M. Z., BAŞKAN, C., GÖKÇE, S. E. (2012). Congenital Heterochromia: A Case Report. Acta Oncologica Turcica, Cilt: 45 Sayı: 1, 18–20. https://ajindex.com/articles/978792

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