Lisch W
Klin Monbl Augenheilkd. 1976 Feb;168(02):228-31.
The alterations characteristic for Iridoschisis (type I and II) are discussed in the light of our own observations. Iridoschisis must be differentiated from the essential progressive iris atrophy, from the dysgenesis mesodermalis corneae et iridis (Rieger), the Chandler syndrome and from the genuine polycoria. Because of the genetic inter-relationships between Iridoschisis, essential promalis corneae and iridis, a predisposition for the occurrence of these alterations has to be taken into account.
根据我们自己的观察结果，讨论了虹膜劈裂症（I型和II型）的特征性改变。虹膜劈裂症必须与原发性进行性虹膜萎缩、中胚层性角膜虹膜发育异常（里格尔综合征）、钱德勒综合征以及真性多瞳症相鉴别。由于虹膜劈裂症、原发性角膜虹膜进行性病变之间存在遗传相关性，因此必须考虑发生这些改变的易感性。
