Morphological and Functional Correlates in Goldmann-Favre Syndrome: A Case Series
Korean Journal of Ophthalmology
;
: 143-146, 2012.
Artigo
em Inglês
| WPRIM
| ID: wpr-40415
ABSTRACT
The purpose of this study is to describe the correlation of findings between results from spectral domain optical coherence tomography (SD-OCT) and microperimetry in a case series regarding patients with Goldmann-Favre syndrome. Goldmann-Favre syndrome is a rare autosomal recessive hereditary vitreo-retinal degeneration that impacts the functionality of vision in subjects. Three men with this condition were assessed and subjected to microperimetry and SD-OCT. Two of the men were brothers. This study finds that the retinoschisis and macular cystoid changes noted in the SD-OCT matched the scotomas revealed by the microperimetry. The findings of each of the individual cases are reported herein.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Escotoma
/
Oftalmopatias Hereditárias
/
Edema Macular
/
Retinosquise
/
Tomografia de Coerência Óptica
/
Testes de Campo Visual
Limite:
Adulto
/
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Korean Journal of Ophthalmology
Ano de publicação:
2012
Tipo de documento:
Artigo
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