Faruk İNCECİK, Özlem SANGÜN, Cenk AKÇALI, Ertap AKOĞLU, Lütfü SAVAŞ, Esin ATİK

Keratit-iktiyozis-sağırlık sendromu: Vaka sunumu

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.

Anahtar Kelimeler:

Ergen, Keratit, İktiyozis, Kadın, Sağırlık

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

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.

Keywords:

Adolescent, Keratitis, Ichthyosis, Female, Deafness,

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