Journals / Çocuk Dergisi / 2007 / Cilt: 7 - Sayı: 3

Keratitis-ichthyosis-deafness (KID) Syndrome: A case report

Keratit-iktiyozis-sağırlık sendromu: Vaka sunumu

Pages
210–212
DOI
—
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AI Summary & Key Takeaways

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

This case is presented in order to point out to the different features of this rare syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Thirteen years-old girl patient with keratitis, ichthyosis, and deafness (KID) syndrome is presented.
📊
Key Findings & Data:Hair, nail and tooth abnormalities are the additional clinical features of the disease.
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Conclusion & Impact:This case is presented in order to point out to the different features of this rare syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ergen · Keratit · İktiyozis

Abstract

Thirteen years-old girl patient with keratitis, ichthyosis, and deafness (KID) syndrome is presented. Hair, nail and tooth abnormalities are the additional clinical features of the disease. Although keratitis is an important component of the triad of KID syndrome, this patient has other ophthalmologic signs like photophobia and bilateral conjunctival infection. This case is presented in order to point out to the different features of this rare syndrome.

Özet

Onüç yaşında keratit, iktiyoz sağırlık (Keratitis-Ichthyosis-Deafness=KID) sendromu tanısı konmuş bir kız çocuğu sunulmaktadır. Hastalığa eşlik eden klinik bulgular, saç, tırnak ve diş anomalileridir. Keratit, KID sendromunun önemli bir komponenti olmakla birlikte, hastamızın fotofobi ve bilateral konjenktival infeksiyon gibi farklı oftalmolojik bulguları bulunmaktaydı. Vaka, bu ender görülen sendromun farklı klinik özelliklerine dikkat çekmek için sunulmuştur.

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Cite This Article

İNCECİK, F., SANGÜN, Ö., AKÇALI, C., AKOĞLU, E., SAVAŞ, L., ATİK, E. (2007). Keratitis-ichthyosis-deafness (KID) Syndrome: A case report. Çocuk Dergisi, Cilt: 7 - Sayı: 3, 210–212. https://ajindex.com/articles/156933

References (10)

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