本综合症是一种罕见的常染色体隐性遗传为特征的先天性疾病。1939年Nakajo首先报告2例。至1985年仅有日本杂志上报道过11例。为使世界各地皮肤科医师对这个稀有的综合症引起注意,本文复习既往病例,并报告第12例如下: 1981年7月一个5岁男孩因再发性红斑和上肢萎缩症而首次就诊。除祖父母近亲结婚 This syndrome is a rare congenital autosomal recessive disease characterized by. Nakajo first reported two cases in 1939. By 1985, only Japanese journals reported 11 cases. To draw the attention of dermatologists around the world to this rare syndrome, this article reviews previous cases and reports the twelfth example as follows: A 5-year-old boy was first seen in July 1981 for recurrent erythema and upper extremity atrophy. In addition to grandparents get married