Sturge-Weber综合征又称脑三叉神经血管瘤病、特点为面部血管痣、对侧限局性抽搐、偏瘫,同侧颅内钙化及不同程度的智力低下。我院收治1例,兹报告如下。患者男性,22岁.发作性左半身抽搐21年,1983年1月28日就诊.患者系第3胎足月顺产.出生后即见右额面部红斑.7月龄始发作性左半身抽搐,发作自左下肢开 Sturge-Weber syndrome, also known as brain trigeminal hemangiomatosis, is characterized by facial nevus, lateral convulsions, hemiparesis, ipsilateral intracranial calcification and mental retardation to varying degrees. A hospital admitted to our hospital, it is reported as follows. Patient, male, 22 years old, episodic left-sided seizures for 21 years, January 28, 1983. The patient was born on the third day of full-term pregnancy. , Seizures since the left lower limb open