Norrie disease

A rare X-linked genetic vitreoretinal condition characterized by abnormal retinal development with congenital blindness. Common associated manifestations include sensorineural hearing loss and developmental delay, intellectual disability and/or behavioral disorders.

Also known as: Episkopi blindness, Norrie disease, Norrie disease, X-linked recessive, Norrie-Warburg disease, atrophia bulborum hereditaria, Anderson-Warburg syndrome, ND, NDP

21 clinical trials for this condition and its sub-types.