Wilms H, Back E, Kirste G
Klin Wochenschr. 1986 Sep 1;64(17):800-3. doi: 10.1007/BF01732191.
Missing iris combined with debility and incidence of Wilms' tumor seem to be a complex syndrome which appears in 1:100,000 people. It is caused by an interstitial deletion on the short arm of chromosome no. 11. We refer to a patient who developed end-stage renal failure caused by a focal-segmental nephrosclerosis. He underwent renal transplantation because chronic hemodialysis was impossible due to his lack of compliance. The deletion of chromosome 11 could be recognized by chromosomal analysis after transplantation. An aniridia-Wilms' tumor association (AWTA) with following focal segmental nephrosclerosis could be diagnosed.
虹膜缺失合并虚弱以及肾母细胞瘤的发病率似乎是一种复杂综合征,每10万人中就有1人出现。它是由11号染色体短臂的间质缺失引起的。我们提到一位因局灶节段性肾小球硬化导致终末期肾衰竭的患者。由于他不配合,无法进行慢性血液透析,因此接受了肾移植。移植后通过染色体分析可识别出11号染色体的缺失。可诊断出伴有局灶节段性肾小球硬化的无虹膜-肾母细胞瘤关联综合征(AWTA)。