摘要
报告一例Waardenburg综合征,表现为先天性聋哑、鼻根粗大、并眉、虹膜异色、眼底色素少,无眦部异位。为散发病例,但其一位姨表弟患眼皮肤白化病。
We report a patient with Waardenburg syndrome. He suffers from congenital deafness and presents high broad nasal root, synophrys, iris heterochromia and fundus hypopigment. The dystopia canthus is absence. In his family pedigree analysis, we found that his second cousin has oculocutaneous albinism.
出处
《眼科学报》
1991年第4期196-198,171,共4页
Eye Science
