Your browser doesn't support javascript.
loading
Fovea Plana in a 9-Year-Old Boy Presenting with Decreased Vision in the Left Eye.
Bechet, Lorane; Hage, Rabih; Vest, Agathe; Jean-Charles, Albert; Merle, Harold.
Afiliação
  • Bechet L; Department of Ophthalmology, University Hospital of Fort de France, Fort de France, Martinique.
  • Hage R; Department of Ophthalmology, University Hospital of Fort de France, Fort de France, Martinique.
  • Vest A; Department of Ophthalmology, University Hospital of Fort de France, Fort de France, Martinique.
  • Jean-Charles A; Department of Ophthalmology, University Hospital of Fort de France, Fort de France, Martinique.
  • Merle H; Department of Ophthalmology, University Hospital of Fort de France, Fort de France, Martinique.
Am J Case Rep ; 20: 537-541, 2019 Apr 17.
Article em En | MEDLINE | ID: mdl-30995212
ABSTRACT
BACKGROUND Foveal hypoplasia (FH) is a congenital disorder, generally associated with other conditions. CASE REPORT A 9-year-old boy presented with moderately decreased vision in the left eye. Fundus examination showed an absence of macular reflection and no foveal pit was seen on optical coherence tomography. Fluorescein angiography demonstrated the absence of a foveal avascular zone. CONCLUSIONS This is a rare case of a unilateral fovea plana associated with a visual impairment.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Baixa Visão / Nistagmo Congênito / Fóvea Central Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Revista: Am J Case Rep Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oftalmopatias Hereditárias / Baixa Visão / Nistagmo Congênito / Fóvea Central Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Male Idioma: En Revista: Am J Case Rep Ano de publicação: 2019 Tipo de documento: Article