ORPHA:891
Familial exudative vitreoretinopathy
Also called Criswick-Schepens syndrome, FEVR
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:891 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Peripheral retinal avascularization
- Falciform retinal fold
- Reduced visual acuity
- Tractional retinal detachment
- Abnormality of the optic disc
- Retinal neovascularization