Ocular Findings in Cri Du Chat Syndrome: A Case Report
Journal of the Korean Ophthalmological Society
;
: 1867-1870, 2008.
Artículo
en Coreano
| 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. CASESUMMARY:
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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Polienos
/
Atrofia Óptica
/
Exotropía
/
Anomalías Craneofaciales
/
Síndrome del Maullido del Gato
/
Hipertelorismo
Tipo de estudio:
Estudio diagnóstico
Límite:
Humanos
/
Lactante
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
2008
Tipo del documento:
Artículo
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