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- B0e33bd7d209b9f80ae31c51f18e19aae hasDbXref "Orphanet:25968" @default.
- B0e33bd7d209b9f80ae31c51f18e19aae type Axiom @default.
- B0e33bd7d209b9f80ae31c51f18e19aae annotatedProperty IAO_0000115 @default.
- B0e33bd7d209b9f80ae31c51f18e19aae annotatedSource MONDO_0007558 @default.
- B0e33bd7d209b9f80ae31c51f18e19aae annotatedTarget "Benign occipital epilepsy is a rare, genetic neurological disorder characterized by visual seizures and occipital epileptiform paroxysms reactive to ocular opening which present in infancy to mid-adolescence. Vomiting, tonic eye deviation and impairment of consciousness are typically associated with the Panayiotopoulos type, while visual hallucinations, ictal blindness and post-ictal headache are commonly observed in the Gastaut type. Electroencephalographic findings in both types are similar and include bilateral, synchronous, high voltage spike-wave complexes in a normal background activity located predominantly in the occipital lobes." @default.