Koster R, van Balen A T
Ophthalmic Paediatr Genet. 1985 Aug;6(1-2):241-6.
A case history of a newborn infant is discussed. At birth he showed bilateral buphthalmos with aniridia and congenital corneal opacities, agreeing with Peters' anomaly. A keratoplasty was performed. The dysgenesis mesenchymalis classification is mentioned briefly. High resolution banding technique of chromosomes revealed no abnormality.
讨论了一名新生儿的病例史。出生时,他表现出双眼牛眼、无虹膜和先天性角膜混浊,符合彼得斯异常。进行了角膜移植术。简要提及了间充质发育异常的分类。染色体高分辨率显带技术未发现异常。