De novo KCNQ2 mutations in patients with benign neonatal seizures

被引：45
|
作者：
Claes, LRF
Ceulemans, B
Audenaert, D
Deprez, L
Jansen, A
Hasaerts, D
Weckx, S
Claeys, KG
Del-Favero, J
Van Broeckhoven, C
De Jonghe, P
机构：
[1] Univ Antwerp, Dept Mol Genet, B-2020 Antwerp, Belgium
[2] Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium
[3] Epilepsy Ctr Children & Youth, Pulderbos, Belgium
[4] Univ Hosp VUB, Dept Neurol, Brussels, Belgium
来源：
NEUROLOGY | 2004年 / 63卷 / 11期
关键词：
D O I：
10.1212/01.WNL.0000145629.94338.89
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Benign familial neonatal convulsions (BFNC) are characterized by unprovoked seizures during the first weeks of life with spontaneous remission after a few months. Mutations have been identified in the voltage-gated potassium ion channels KCNQ2 and KCNQ3. The authors performed a mutation analysis of KCNQ2 and KCNQ3 in six patients of whom four had no family history of neonatal seizures. The authors identified three KCNQ2 mutations in four patients that all arose de novo.
引用
收藏
页码：2155 / 2158
页数：4
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