Koch P, Foss P, Baum H P, Zaun H
Hautklinik Universität des Saarlandes, Homburg/Saar.
Hautarzt. 1995 Apr;46(4):272-5. doi: 10.1007/s001050050254.
We report on a 23-year-old man with hidrotic ectodermal dysplasia of the Clouston type showing a severe expression of his gene defect. As a prominent feature of this case, we describe the presence of verruciform keratoderma of hands and feet, and we visualize these skin changes by means of a new imprinting technique.
我们报告了一名23岁患有克劳斯顿型汗孔角化性外胚层发育不良的男性,其基因缺陷表现严重。作为该病例的一个突出特征,我们描述了其手足疣状角化病的存在,并通过一种新的印记技术将这些皮肤变化可视化。