Two Cases of Isolated Foveal Hypoplasia
Journal of the Korean Ophthalmological Society
;
: 1224-1229, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-62248
ABSTRACT
Foveal hypoplasia has been described in association with aniridia, albinism, microphthalmia and achromatopsia. Isolated foveal hypoplasia unassociated with other ocular abnormalities has been rarely reported and is regarded as a rare condition. Authors experienced two cases of isolated foveal hypoplasia in the same family. A 30-year-old woman and her 3-year-old daughter presented with a complaint of poor visual acuity and nystagmus. Ophthalmoscopic examination of their both eyes revealed loss of foveal reflex, absence of macular luteal pigment, and abnormal distribution of retinal vessels at the posterior pole. No abnormal ocular findings other than lens opacity, high myopia, and large optic cup were found.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Reflexo
/
Vasos Retinianos
/
Catarata
/
Núcleo Familiar
/
Acuidade Visual
/
Aniridia
/
Albinismo
/
Microftalmia
/
Defeitos da Visão Cromática
/
Miopia
Limite:
Adulto
/
Criança, pré-escolar
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1996
Tipo de documento:
Artigo
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