Benign paroxysmal tonic upgaze of childhood with ataxia

A rare paroxysmal movement disorder characterized by episodes of sustained, conjugate, upward deviation of the eyes and down beating saccades in attempted downgaze (with preserved horizontal eye movements) which is accompanied by ataxic symptomatology (unsteady gait, lack of balance and movement coordination disturbances) in an otherwise healthy individual. Bilateral vertical nystagmus is associated. Symptoms generally disappear spontaneously within 1-2 years after onset.

Also known as: Ouvrier-Billson syndrome, neuroocular syndrome 2, paroxysmal type, Ouvrier Billson syndrome, paroxysmal tonic upgaze, benign childhood, with ataxia

12 clinical trials for this condition and its sub-types, 0 tagged with Benign paroxysmal tonic upgaze of childhood with ataxia itself.