{"orpha":25968,"name":"OBSOLETE: Self-limited childhood occipital epilepsy","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Benign occipital epilepsy"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Childhood-onset epilepsy syndrome","url":"https://raremap.alftech.space/d/ORPHA-25968/","orphanet_url":"https://www.orpha.net/en/disease/detail/25968","names":{"fr":{"name":"OBSOLETE : Epilepsie occipitale autolimitée de l'enfance","synonyms":["OBSOLETE : Epilepsie occipital auto-résolutive de l'enfance","OBSOLETE : Epilepsie à pointes occipitales"]},"de":{"name":"OBSOLET: Selbstlimitierende okzipitale Epilepsie im Kindesalter","synonyms":["OBSOLET: Benigne okzipitale Epilepsie"]},"es":{"name":"OBSOLETO: Epilepsia occipital infantil autolimitada","synonyms":["OBSOLETO: Epilepsia occipital benigna"]},"it":{"name":"OBSOLETO: Epilessia occipitale autolimitante dell'infanzia"},"nl":{"name":"OBSOLEET: Zelflimiterende occipitale epilepsie in de kindertijd","synonyms":["OBSOLEET: Goedaardige occipitale epilepsie"]},"pt":{"name":"OBSOLETO: Epilepsia occipital auto-limitada da infância","synonyms":["OBSOLETO: Epilepsia occipital benigna"]},"pl":{"name":"NIEAKTUALNE: Łagodna padaczka potyliczna","synonyms":["OBSOLETE: Benign occipital epilepsy"]},"cs":{"name":"NEAKTUÁLNÍ: Benigní okcipitální epilepsie","synonyms":["OBSOLETE: Benign occipital epilepsy"]},"uk":{"name":"Доброякісна потилична епілепсія","definition":"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."},"zh":{"name":"良性枕叶癫痫"},"tr":{"name":"Selim oksipital epilepsi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98259,"name":"Childhood-onset epilepsy syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}