Nass R, Devinsky O
New York University Medical Center, Department of Neurology, NYC 10016, USA.
Neuropsychiatry Neuropsychol Behav Neurol. 1999 Jul;12(3):193-7.
This study was designed to further define the electroencephalographic abnormalities seen in the Landau-Kleffner syndrome variants and the associated clinical features.
Landau-Kleffner syndrome is rare, but its putative variants are more common.
We report two patients with centro-temporal spikes, autistic epileptiform regression, and variably prominent oro-motor symptoms.
The epileptic aphasia pattern found among patients with prominent Rolandic spikes may more frequently involve expressive language than is seen in the typical Landau-Kleffner syndrome, where verbal auditory agnosia is the rule.
This clinical difference likely reflects the location of the epileptiform activity (centrotemporal as opposed to anterior or mid-temporal) on buccal-lingual function, vocalization, and language production.
本研究旨在进一步明确Landau-Kleffner综合征变异型中出现的脑电图异常及相关临床特征。
Landau-Kleffner综合征罕见,但其假定的变异型更为常见。
我们报告了两名患有中央颞区棘波、自闭症样癫痫性退化以及不同程度显著口面部运动症状的患者。
在具有显著罗兰多棘波的患者中发现的癫痫性失语模式可能比典型的Landau-Kleffner综合征更常累及表达性语言,典型的Landau-Kleffner综合征以言语听觉失认症为特征。
这种临床差异可能反映了癫痫样活动的位置(中央颞区而非颞叶前部或中部)对颊舌功能、发声和语言产生的影响。