Doose H, Brigger-Heuer B, Neubauer B
Epilepsy Center, Epilepsy Research Unit, Raisdorf, Germany.
Epilepsia. 1997 Jul;38(7):788-96. doi: 10.1111/j.1528-1157.1997.tb01466.x.
To investigate the spectrum of clinical manifestations in children with benign focal sharp waves in the EEG to gain further insight into the genetic background of clinical and EEG symptomatology in a family study.
All 147 children (134 with seizures, 13 without) met the following inclusion criteria: (a) at least one EEG with focal sharp waves characteristic of benign partial epilepsies, and (b) at least 1 sibling investigated by EEG. The families were questioned orally or in writing regarding the occurrence of seizures. Patients' records were evaluated by a standardized scheme.
The following types of seizures occurred: febrile convulsions (FC), afebrile generalized tonic-clonic seizures (GTCS), simple and (rarely) complex partial seizures; and rolandic seizures in the strict sense. Neonatal seizures were overrepresented (6%); there were no indications of lesional causes. FC occurred in 38 children (26%). As compared with unselected cases of FC, complex symptoms were overrepresented. Family data suggested a maternal preponderance in the transmission of FC liability. Affected relatives of FC probands manifested FC more often than did relatives of probands without FC. Families of 32 patients with typical rolandic seizures (24% of the 134 probands with seizures) showed no aggregation of rolandic epilepsy, but did show variable seizure types. In the entire sample, EEG investigations showed focal sharp waves in 11% of siblings aged 2-10 years. No relation existed between clinical symptomatology and sharp wave findings in siblings. In 66% of probands, the EEG disclosed generalized genetic patterns. Siblings with generalized spike-waves (sw) and/or theta rhythm had focal sharp waves more often than those without sw and/or theta rhythm.
The phenotypic expression of the genetic anomaly underlying focal sharp waves shows considerable variability. The clinical and EEG findings are in agreement with a multifactorial pathogenesis of epilepsies with "benign" focal epileptiform sharp waves.
研究脑电图(EEG)显示良性局灶性尖波的儿童的临床表现谱,以便在一项家系研究中进一步深入了解临床和EEG症状学的遗传背景。
147名儿童(134名有癫痫发作,13名无癫痫发作)均符合以下纳入标准:(a)至少有一次脑电图显示具有良性部分性癫痫特征的局灶性尖波,(b)至少有一名同胞接受了脑电图检查。通过口头或书面询问这些家庭癫痫发作的情况。患者的记录采用标准化方案进行评估。
出现了以下几种癫痫发作类型:热性惊厥(FC)、无热全身性强直阵挛发作(GTCS)、简单部分性发作和(罕见的)复杂部分性发作;以及严格意义上的罗兰多癫痫发作。新生儿癫痫发作的比例过高(6%);没有病变原因的迹象。38名儿童(26%)出现了热性惊厥。与未选择的热性惊厥病例相比,复杂症状的比例过高。家系数据表明,热性惊厥易感性的传递以母系为主。热性惊厥先证者的受影响亲属比无热性惊厥先证者的亲属更常出现热性惊厥。32例典型罗兰多癫痫发作患者的家系(134例癫痫先证者中的24%)未显示罗兰多癫痫的聚集性,但确实显示出多种发作类型。在整个样本中,脑电图检查显示2至10岁的同胞中有11%出现局灶性尖波。同胞的临床症状学与尖波发现之间没有关联。在66%的先证者中,脑电图显示出全身性遗传模式。有全身性棘波(sw)和/或θ节律的同胞比没有sw和/或θ节律的同胞更常出现局灶性尖波。
局灶性尖波潜在的遗传异常的表型表达具有相当大的变异性。临床和脑电图结果与具有“良性”局灶性癫痫样尖波的癫痫的多因素发病机制一致。