Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease

Norrie disease is a recessive x-linked genetic disorder (MIM# 310600) that is associated with early childhood blindness due to vascular proliferative changes in the retina, as well as cognitive impairment, seizures, and sometimes sensorineural hearing loss with onset later in life. We describe here a 45-year-old Finnish male with Norrie disease, who lived in a nursing home due to visual impairment, learning disability, and epilepsy and was...