Kiesewetter F, Simon M, Fartasch M, Gevatter M
Department of Dermatology, University of Erlangen-Nürnberg, FRG.
Dermatology. 1993;186(3):222-5. doi: 10.1159/000247351.
An atypical case of the rare genodermatosis erythrokeratodermia progressiva partim symmetrica (EPPS) with deafness and myopathy is described. Our findings suggest that this case of EPPS with deafness and myopathy represents a distinct entity of atypical erythrokeratodermias with characteristic epidermal and dermal skin changes.
描述了一例罕见的进行性对称性部分性红皮角化病（EPPS）合并耳聋和肌病的非典型病例。我们的研究结果表明，这例伴有耳聋和肌病的EPPS代表了一种具有特征性表皮和真皮皮肤改变的非典型红皮角化病的独特实体。
