Literature DB >> 10840404

Early recognition of benign partial epilepsy in infancy.

A Okumura1, F Hayakawa, T Kato, K Kuno, T Negoro, K Watanabe.   

Abstract

PURPOSE: The aim of this study is to determine how precisely we can recognize the outcome in infants with epilepsy beginning in the first year of life.
METHODS: We performed a prospective 5-year follow-up study on 63 patients who developed epilepsy in the first year of life. We first judged that patients met the criteria of "possible benign partial epilepsy in infancy (BPEI)" on enrollment in this study. At 2 years of age, we reevaluated the seizure and developmental outcome in the patients who were diagnosed as having "possible BPEI." We finally judged that patients met the criteria of "definite BPEI" at age 5 years. "Possible BPEI" was defined as epilepsy meeting all the following conditions: (a) complex partial seizures and/or secondarily generalized seizures; (b) normal psychomotor development and neurologic findings before onset; (c) normal interictal electroencephalograms; (d) normal cranial computed tomography (CT) and magnetic resonance imaging (MRI) findings; and (e) no seizures during the first 4 weeks of life. "Definite BPEI" was defined as epilepsy meeting all the following criteria in addition to those of "possible BPEI": (a) normal psychomotor development beyond age 5 years, and (b) no seizures beyond age 2 years.
RESULTS: Thirty-two of the 63 patients met the inclusion criteria completely and were included in the "possible BPEI" group. Twenty-five of the 32 patients completed the 5-year follow-up. At age 2 years, four patients were excluded from the "possible BPEI" group because of seizure recurrence and/or delayed development. By age 5 years, one had a recurrence of seizures, and another exhibited mildly delayed psychomotor development. We finally diagnosed 19 patients as having "definite BPEI." "Definite BPEI" accounted for 76% of the patients diagnosed as having "possible BPEI" at the first presentation and 90% of those who met the conditions on reevaluation at age 2 years.
CONCLUSIONS: Recognition of BPEI is possible, to some extent, at the first presentation, and reevaluation at age 2 years is useful for a more precise diagnosis.

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Mesh:

Year:  2000        PMID: 10840404     DOI: 10.1111/j.1528-1157.2000.tb00233.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  3 in total

1.  Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families.

Authors:  Jialinzi He; Haiyun Tang; Chaorong Liu; Langzi Tan; Wenbiao Xiao; Bo Xiao; Hongyu Long; Lili Long
Journal:  Exp Ther Med       Date:  2021-03-18       Impact factor: 2.447

2.  Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.

Authors:  Xiaoling Yang; Yuehua Zhang; Xiaojing Xu; Shuang Wang; Zhixian Yang; Ye Wu; Xiaoyan Liu; Xiru Wu
Journal:  BMC Neurol       Date:  2013-12-26       Impact factor: 2.474

3.  Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Authors:  Qi Zeng; Xiaoling Yang; Jing Zhang; Aijie Liu; Zhixian Yang; Xiaoyan Liu; Ye Wu; Xiru Wu; Liping Wei; Yuehua Zhang
Journal:  J Hum Genet       Date:  2017-11-13       Impact factor: 3.172

  3 in total

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