本症候群从1952年报告以来,大多文献指出,该症多见于男孩,以X—因子隐性遗传的方式发病,女孩世界上仅有数例报告。笔者观察一例报告如下。男性,7岁8个月。家族史:双亲间无血缘关系。兄姐各一人健在,其他直系亲属中无特殊疾病记载。病史:足月顺产,生后3个月精神活动与身体发育一致。4个月时,因“眼内积水”,手术。 Since the 1952 report, most of the literature pointed out that this syndrome is more common in boys than in boys, with X-factor recessive inheritance. There are only a few cases reported in girls in the world. The author observed a case report is as follows. Male, 7 years and 8 months. Family history: no relationship between parents. Sister each one is alive, other immediate family members without special disease records. History: full-term natural delivery, 3 months after birth mental activity and body development consistent. 4 months, due to “eye water” surgery.