Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja 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. Disease data Klasyfikacja Clinical syndrome Synonimy Cortical visual impairment Korowe uszkodzenie wzroku Kod ORPHA 447788 Kod OMIM - Kod ICD10 H47.6 Kod ICD11 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl