Komoto综合征又称睑裂综合征，是一种常染色体显性遗传性疾病。其主要特征为双侧睑裂狭窄、上睑下垂、内毗反向资皮和内毗间距增定。对于本症的手术治疗实际包括内毗远距及内毗赘皮的矫正，外姚成形及上睑下垂矫正3个手术。目前已有3个手术一次完成的报道。我们采用Bla。k。vie Komoto syndrome, also known as blepharophimosis syndrome, is an autosomal dominant genetic disease. The main features of bilateral palpebral fissure stenosis, ptosis, the inner adjacent to the reverse of the inner skin and the adjacent pitch increase. Surgical treatment of this disease, including the actual treatment of the remote and within the epicanthosis correction, the formation of Yao and ptosis surgery three. There are currently three reports of one completed surgery. We use Bla. k. vie