| 2 | 先天性血管萎缩性皮肤异色症并发汗孔角化症及双侧虹膜发育不全的特殊病例1例显示文摘Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive genodermatosis characterized by poikiloderma and the variable presence of other features including skeletal and ocular abnormalities, ectodermal defects, and suscept-ibility to certain malignancies. We report a 40-year-old woman with known RTS who developed porokeratoses on her limbs in adulthood, an association that has not previou-sly been reported. In addition, she had bilateral iris dysgenesis, which has only been described once before in RTS. | Mak R.K.H. Griffiths W.A.D. Mellerio J.E. 吴佳纹 | 2006 | 世界核心医学期刊文摘(皮肤病学分册)2006，0，5： | 0 |
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