Goldmann-Favre syndrome

Abstract

Goldmann-Favre syndrome is a rare autosomal recessive vitreoretinal dystrophy that appears usually during childhood, and it manifests with progressive loss of visual acuity, night blindness, and poor color recognition. Fundus findings include degenerative pigmentary changes with macular edema and retinoschisis.

Keywords

• enhanced s-cone
• goldmann-favre
• lamellar macular hole