Velkey I, György I
Borsod-Abaúj-Zemplén Megyei Kórház-Rendelöintézet, Miskolc.
Orv Hetil. 1992 May 3;133(18):1117-8.
Authors report about a girl with Landau-Kleffner syndrome. After the history of normal developmental milestones at the age of five-and-half year the patient had absence seizures, and marked receptiv and expressiv aphasia developed gradually. She was found to have Landau-Kleffner syndrome. This entity initially can be regarded as deafness or psychiatric reaction. The seizure activity usually has a favorable outcome, the aphasia can fluctuate for years. The improvement is more likely in promptly treated cases.
作者报告了一名患有 Landau-Kleffner 综合征的女孩。在五岁半时发育里程碑正常的病史之后，该患者出现失神发作，并逐渐发展为明显的感受性和表达性失语。她被诊断为 Landau-Kleffner 综合征。这种病症最初可能被视为耳聋或精神反应。癫痫发作活动通常预后良好，失语可能会持续数年波动。及时治疗的病例更有可能改善。
