Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare developmental defect during embryogenesis characterized by unilateral duplication of an eye which may appear as a synophthalmic eye in a single orbit or as two separate unilateral eyes, each in a separate orbit. The malformation is always associated with other anomalies of the central nervous system (such as porencephaly, meningocele, or arachnoidal cysts) and with craniofacial abnormalities. A proboscis is often found. Clinically, moderate mental retardation and epilepsy are typical. Disease data Klasyfikacja Morphological anomaly Synonimy Jednostronne zdwojenie oka Triophthalmia Triopia Unilateral diplophthalmia Unilateral diplophthalmos Kod ORPHA 3374 Kod OMIM - Kod ICD10 Q15.8 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