Cerebral visual impairment
ORPHA:447788· ICD-10 H47.6
Definition
A rare neurologic disease characterized by significant visual dysfunction that cannot be explained by ocular abnormalities alone and is due to damage to post-chiasmatic visual pathways and structures during early perinatal development. Signs and symptoms include decreased visual acuity, visual field defects, and impairments in visual processing and attention.
- Prevalence
- Unknown
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal