Year-end Sale % OFF 
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.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
