Late-onset childhood occipital epilepsy (Gastaut type): A family study

被引:7
|
作者
Grosso, Salvatore [1 ]
Vivarelli, Rossella [1 ]
Gobbi, Giuseppe [2 ]
Di Bartolo, Rosanna [1 ]
Berardi, Rosario [1 ]
Balestri, Paolo [1 ]
机构
[1] Univ Siena, Dept Pediat, Pediat Neurol Sect, Siena Santa Maria Scotte Hosp, I-53100 Siena, Italy
[2] Maggiore A Pizzardi Hosp, Bologna, Italy
关键词
epilepsy; partial seizures; occipital lobe epilepsy;
D O I
10.1016/j.ejpn.2007.11.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Late onset childhood occipital epilepsy-Gastaut type (LOCOE) is a rare idiopathic epilepsy syndrome with an uncertain long-term prognosis, Elementary visual hallucinations and interictal spike-and-wave complexes in the occipital areas represent the main electroclinical findings of the syndrome, The functional nature of LOCOE has been emphasized together with the presence of genetic predisposition in the affected patients. Here, we report on two families in which two patients, respectively, showed electroclinical features compatible with LOCOE. Although further studies are needed to validate our observations, the involvement of two generations in one of the families we studied may corroborate the previously formulated hypothesis of an autosomal dominant model of inheritance in LOCOE. Of course, the identification of larger families is propaedeutic to linkage analysis studies. (C) 2007 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:421 / 426
页数:6
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