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本文报告100例儿童结节硬化综合症(以下简称TSS)的早期临床和脑电图特点,着重癫痫表现和皮肤改变的个体变化。男性61例,女性39例,详细病史包括家族史、生产史、导致病人首次来神经科就医的症状发展等。对数月内初生婴儿的诊断则通过足够的随诊后才确定。脑电图常在数周、数月或数年后反复记录,1957年—1971年中共进行了525次脑电图检查。资料有些来源于婴儿痉挛综合征伴运动与精神发育迟缓者,有些由于其他型发作或精神缺损者。对皮肤病损给以特别的注意,尤其是躯干或肢体任何部位的
This paper reports the early clinical and electroencephalographic features of 100 children with nodular sclerosis (TSS), focusing on individual changes in epilepsy and skin changes. There were 61 males and 39 females. The detailed history includes family history and production history, leading to the patient’s first visit to neurology and other symptoms. The diagnosis of newborn infants within months is confirmed by adequate follow-up. The EEG is often recorded several weeks, months or years later, and from 1957 to 1971, the CCP conducted 525 EEG examinations. Some sources of information from infantile spasms associated with exercise and mental retardation, and some due to other types of seizures or mental deficiencies. Give special attention to skin lesions, especially in any part of the trunk or limb