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Ocular Findings in Cri Du Chat Syndrome: A Case Report
Journal of the Korean Ophthalmological Society ; : 1867-1870, 2008.
Article in Korean | WPRIM | ID: wpr-198092
ABSTRACT

PURPOSE:

To report the ophthalmologic examination of an infant who has cri du chat syndome with exotropia and facial abnormalities. CASE

SUMMARY:

A 7 - month - old infant was confirmed as having cri du chat syndrome by a chromosomal study. He showed mild developmental retardation and eyeball deviation. This male infant underwent ophthalmic evaluations, including an extraocular examination, measurement of deviation, ocular movement test, interepicanthal distance, and fundus examination. As a result, facial abnormalities were found, including telecanthus and epicanthal folds. The infant had intermittent exotropia of 40 prism diopters according to the Hirschberg test and optic atrophy according to the fundus examination.

CONCLUSIONS:

Cri du chat syndrome manifests with many different ocular symptoms, including hypertelorism, telecanthus, epicanthal folds, and exotropia.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Polyenes / Optic Atrophy / Exotropia / Craniofacial Abnormalities / Cri-du-Chat Syndrome / Hypertelorism Type of study: Diagnostic study Limits: Humans / Infant / Male Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Polyenes / Optic Atrophy / Exotropia / Craniofacial Abnormalities / Cri-du-Chat Syndrome / Hypertelorism Type of study: Diagnostic study Limits: Humans / Infant / Male Language: Korean Journal: Journal of the Korean Ophthalmological Society Year: 2008 Type: Article