本文报告作者所见4例Kleine-Levin综合征。 例1 男,16岁。1974年乙醚麻醉切除阑尾后,苏醒过程中曾有胡言乱语,哭闹不安,历时4～5天。1978～1980年每年发作1次,嗜睡,缄默,少动,历时5～6天。发作前头昏,发作时反复呼唤方醒,食量大,食毕又睡,二便自理。1981年5月、6月各发1次,末次恢复期中入院。无阳性体征或精神异常。血糖、嗜酸细胞计数、胸透、心电图、脑电图、24小时尿VMA含量测定等皆正常;ACTH促发试验前后嗜酸细胞计数均无明显变化。 例2 男,16岁。因发作性贪睡3个多月于1981年10月3日入院。自当年6月28日起,先后发病6 This article reports the authors see 4 cases of Kleine-Levin syndrome. Example 1 male, 16 years old. After anesthesia in 1974 to remove the appendix, the process of awakening had nonsense, crying uneasy, which lasted 4 to 5 days. 1978 ~ 1980 attack 1 times per year, lethargy, silence, less moving, which lasted 5 to 6 days. Before the onset of dizziness, seizures repeatedly called wake up, food intake, food and sleep, two will take care of themselves. In May 1981, June each made 1, the last convalescence admission. No positive signs or mental abnormalities. Blood glucose, eosinophil count, chest X-ray, electrocardiogram, electroencephalogram, 24-hour urine VMA content were all normal; eosinophil count before and after ACTH test did not change significantly. Example 2 male, 16 years old. Due to episodic snooze more than 3 months in October 3, 1981 admission. Since June 28 that year, has onset 6