Coriorretinopatía lacunar como presentación de Síndrome de Aicardi en el lactante

  1. D. Puertas-Bordallo
  2. M. Lozano-Vázquez
  3. B. De Domingo-Barón
  4. M.L. Ruiz-Falcó Rojas
  5. L. González-Gutiérrez-Solana
  6. J. Fernández-Fernández
Revista:
Archivos de la Sociedad Española de Oftalmologia

ISSN: 0365-6691

Ano de publicación: 2007

Volume: 82

Número: 5

Páxinas: 311-314

Tipo: Artigo

DOI: 10.4321/S0365-66912007000500012 DIALNET GOOGLE SCHOLAR lock_openAcceso aberto editor

Outras publicacións en: Archivos de la Sociedad Española de Oftalmologia

Resumo

Clinical case: We report the case of an 81-day-old female infant who was brought to the Emergency Department because of a seizure. At 20 weeks of gestational age she was diagnosed to have agenesis of the corpus callosum, with this being confirmed later by magnetic resonance imaging. Ophthalmological examination of the fundus showed peripapillar chorioretinal lesions (lacunar chorioretinopathy) in both eyes. Discussion: Chorioretinal lacunar and retinal pigment epithelial abnormalities are the basis for the diagnosis of this syndrome.

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