Ophthalmologic findings in child in the Cornelia de Lange syndrome

PURPOSE: Cornelia de Lange syndrome is a rare disease showing characteristic facial appearance, development delay, low birth weight, skeletal anomaly, hirsutism and various ophthalmologic and hearing findings. MATERIAL AND METHODS: We described ophthalmologic problems in 2-year-old girl. RESULTS: We have find arched eyebrows, long lashes, epiphora, ptosis, nystagmus, myopia, and fundus eye changes. CONCLUSIONS: We recommend early ophthalmologic examination in patients with Cornelia de Lange syndrome.