Damian C
Clinica Oftalmologică Craiova.
Oftalmologia. 1992 Oct-Dec;36(4):391-5.
A patient is 18 years old; he presents Peters' anomaly, microcornea, the persisting of papillar membrana, congenital specifying lens for both eyes and atypical iridic coloboma for the right eye. The eye sight is diminished under the limit of practice usefulness for both eyes. The disease is thought to be a mesodermal dysgenesis of the anterior segment having some persisting fetal structures. The absence of such lesions within the same family pleads for the action of a teratogen factor that have belated action during the 4th-5th month of pregnancy.
一名患者18岁；他患有彼得斯异常、小角膜、瞳孔膜持续存在、双眼先天性晶状体异常以及右眼非典型虹膜缺损。双眼视力均下降至实际有用视力范围以下。该疾病被认为是前段中胚层发育异常，伴有一些持续存在的胎儿结构。同一家族中无此类病变表明存在致畸因素，该因素在妊娠第4至5个月期间具有延迟作用。
