{"orpha":166299,"name":"Benign partial epilepsy of infancy with complex partial seizures","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-166299/","orphanet_url":"https://www.orpha.net/en/disease/detail/166299","names":{"fr":{"name":"Epilepsie bénigne partielle de l'enfant avec crises partielles complexes"},"de":{"name":"Benigne Partialepilepsie im Kleinkindalter mit komplexen fokalen Anfällen"},"es":{"name":"Epilepsia parcial benigna del lactante con crisis parciales complejas"},"it":{"name":"Epilessia parziale benigna dell'infanzia con crisi parziali complesse"},"nl":{"name":"Goedaardige partiële epilepsie met complexe partiële insulten op zuigelingenleeftijd"},"pt":{"name":"Epilepsia parcial benigna da infância com convulsões parciais complexas"},"pl":{"name":"Łagodna niemowlęca padaczka częściowa z napadami złożonymi"},"cs":{"name":"Benigní parciální epilepsie dětského věku s komplexními parciálními záchvaty"},"uk":{"name":"Доброякісна фокальна епілепсія раннього дитячого віку зі складними фокальними судомами","definition":"Benign partial epilepsy of infancy with complex partial seizures is a rare infantile epilepsy syndrome characterized by complex partial seizures presenting with motion arrest, decreased responsiveness, staring, automatisms and mild clonic movements, with or without apneas, normal interictal EEG and focal, mostly temporal discharges in ictal EEG. Most often, seizures occur in clusters and have a good response to treatment. Psychomotor development is normal."},"zh":{"name":"婴儿良性部分性癫痫伴复杂部分性发作","definition":"婴儿期良性部分性癫痫伴复杂部分性发作是一种罕见的婴幼儿癫痫综合征，以复杂部分性发作为特征，表现为运动停止、反应性降低、凝视、自动症和轻度阵挛运动，伴或不伴呼吸暂停，发作间期脑电图正常，发作期脑电图以局灶性、暂时性放电为主。大多数情况下，丛集性发作且对治疗反应良好。精神运动发育正常。"},"tr":{"name":"Kompleks kısmi nöbetler ile seyreden selim kısmi süt çocuğu epilepsisi"}},"xrefs":[{"source":"MONDO","code":"0015638","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4749347","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}