{"orpha":166302,"name":"Benign partial epilepsy with secondarily generalized seizures in infancy","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Self-limited infantile epilepsy","url":"https://raremap.alftech.space/d/ORPHA-166302/","orphanet_url":"https://www.orpha.net/en/disease/detail/166302","names":{"fr":{"name":"Epilepsie partielle bénigne du nourrisson avec crises généralisées secondaires"},"de":{"name":"Benigne Partialepilepsie der frühen Kindheit mit sekundär generalisierten Anfällen"},"es":{"name":"Epilepsia parcial benigna del lactante con crisis generalizadas secundarias"},"it":{"name":"Epilessia parziale benigna dell'infanzia con convulsioni generalizzate secondarie"},"nl":{"name":"Goedaardige partiële epilepsie met secundair gegeneraliseerde insulten op zuigelingenleeftijd"},"pt":{"name":"Epilepsia parcial benigna da infância com generalização secundária"},"pl":{"name":"Łagodna padaczka częściowa z wtórnie uogólnionymi napadami w okresie niemowlęcym"},"cs":{"name":"Benigní parciální epilepsie se sekundárně generalizovanými záchvaty v dětství"},"uk":{"name":"Доброякісна фокальна епілепсія раннього дитячого віку з вторинно генералізованими судомами","definition":"Benign partial epilepsy with secondarily generalized seizures in infancy is a rare infantile epilepsy syndrome characterized by seizures presenting with motion arrest and staring. They are followed by generalized tonic-clonic convulsions with normal interictal EEG and focal paroxysmal discharges, followed by generalization in ictal EEG. Seizures usually occur in clusters and are responsive to treatment. Psychomotor development is normal."},"zh":{"name":"婴儿良性部分性癫痫伴继发全身性发作","definition":"良性部分性癫痫伴婴儿期继发性全身性惊厥是一种罕见的婴儿癫痫综合征，其特征是癫痫发作伴运动停止和凝视。随后为全身性强直阵挛性癫痫发作伴发作间期脑电图正常和局灶阵发性放电，之后发作期脑电图泛化。常为成簇发作，对治疗有反应。精神运动发育正常。"},"tr":{"name":"Süt çocuğunda sekonder jeneralize nöbetler ile seyreden selim kısmi epilepsi"}},"xrefs":[{"source":"MONDO","code":"0015639","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4749728","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":306,"name":"Self-limited infantile epilepsy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}