Doç.Dr., Ankara Üniv.Tıp Fak. Göz Hast.ABD.
Goldmann-Favre syndrome is a hereditary vitreoretinal degeneration characterized by night blindness and progressive visual loss with the clinical findings of vitreous and pigment epithelial degeneration, retinoschisis, cataract and ERG abnormalities. This paper reports a case with typical clinical features of Goldmann-Favre syndrome which is a rare entity. Keywords :
Goldmann-Favre syndrome, Vitreoretinal degeneration, Fluorescein angiography, Optical coherence tomography.
