Goldmann–Favre syndrome

Abstract

In this case report, we aim to report a rare case of Goldmann–Favre syndrome with typical findings, as it can be easily misdiagnosed due to rarity of the disease. The case described here is a young male aged 29 years with typical clinical symptoms who presented with defective vision in both eyes for 3 years with a history of defective night vision since childhood. He was diagnosed with Goldmann–Favre syndrome by fundus examination and optical coherence tomography. He was previously diagnosed as atypical retinitis pigmentosa with cystoid macular edema.