Original articleBenign complex partial epilepsies in infancy
References (8)
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Benign partial epilepsies in childhood
Lesional epilepsies with partial seizures
- Yamamoto N, Watanabe K, Negoro T, et al. Complex partial seizures in children: A study of ictal manifestations and...
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Convulsive disorders in the first year of life: Neurological and mental outcome and mortality
Epilepsia
(1978)
Cited by (101)
Uncommon epileptic syndromes in children: a review
2021, SeizurePRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia
2019, SeizureCitation Excerpt :Additionally, an association of BIE with paroxysmal kinesigenic dyskinesia (PKD) has been reported and called infantile convulsions and choreoathetosis [5]. BIE and/or PKD can all be familial, and genetic factors are assumed to be involved [1,2,5]. In 2011, Chen et al. reported that the proline-rich transmembrane protein 2 (PRRT2) gene was responsible for PKD [6].
Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation
2016, Brain and DevelopmentCitation Excerpt :Given these findings, we do not believe our patient’s focal seizures were attributable to DS. BIE was first described by Watanabe et al. [11,12] as focal epilepsy with a favorable outcome beginning in infancy. BIE is a distinct epilepsy syndrome characterized by clusters of focal seizures with an infantile onset (usually three to ten months of age), no identifiable etiological factors, normal interictal EEG and neuroimaging, and normal psychomotor development [3].
Characteristics of patients with benign partial epilepsy in infancy without PRRT2 mutations
2015, Epilepsy ResearchDifficulty of early diagnosis and requirement of long-term follow-up in benign infantile seizures
2015, Pediatric NeurologyGirl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes
2014, Brain and Development