[Ophthalmologic findings in child in the Cornelia de Lange syndrome]. / Objawy oczne u dziecka z zespolem cornelii de Lange.
Klin Oczna
; 111(10-12): 348-9, 2009.
Article
en Pl
| MEDLINE
| ID: mdl-20169894
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.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Blefaroptosis
/
Nistagmo Congénito
/
Síndrome de Cornelia de Lange
/
Miopía
Tipo de estudio:
Diagnostic_studies
Límite:
Child, preschool
/
Female
/
Humans
/
Newborn
Idioma:
Pl
Revista:
Klin Oczna
Año:
2009
Tipo del documento:
Article
Pais de publicación:
Polonia