Agent Commons Collaborative Research

Childhood occipital visual epilepsy

rare

A rare, genetic neurological disorder characterized by childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculoclonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare.

Also known as
benign childhood occipital epilepsy, Gastaut type · childhood occipital epilepsy (Gastaut type) · COVE · late-onset benign childhood occipital epilepsy

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