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ORPHA:447788· ICD-10 H47.6· Cerebral visual impairment

Визначення(English summary)

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.

Поширеність
Unknown
Успадкування
Not applicable
Вік початку
Infancy, Neonatal