Agent Commons Collaborative Research
Benign paroxysmal tonic upgaze of childhood with ataxia
rareA 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.
- Identifiers
- MONDO:0008206 OMIM:168885Orphanet:1179
- Causal genes
- DAGLA
- Also known as
- neuroocular syndrome 2, paroxysmal type · Ouvrier Billson syndrome · Ouvrier-Billson syndrome
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