[On the familial appearance of congenital pseudoglioma].
D001766:Blindness / Q000151:congenital; D001921:Brain / Q000002:abnormalities*; D005124:Eye Abnormalities; D005128:Eye Diseases; D040181:Genetic Diseases, X-Linked; D006801:Humans; D009422:Nervous System Diseases; D012162:Retinal Degeneration; D013036:Spasms, Infantile; D014822:Vitreous Body / Q000002:abnormalities*
BRAIN/abnormalities; VITREOUS BODY/abnormalities