Gilaberte M, Puig L, Vidal D, Alomar A
Department of Dermatology, Hospital de la Santa Creu i Sant Pau, Av Sant Antoni M Claret, 167, 08025 Barcelona, Spain.
J Eur Acad Dermatol Venereol. 2003 Mar;17(2):196-9. doi: 10.1046/j.1468-3083.2003.00604.x.
Darier's disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Several patients with unilateral, linear, 'zosteriform' or localized lesions have been reported. We report three cases of DD in a localized pattern corresponding to mosaicism type 1 according to Happle's classification and review the literature about the genetic cause of DD and DD in a 'zosteriform' pattern.
达里埃病(DD)是一种常染色体显性遗传性皮肤病,其特征为表皮细胞间黏附丧失和异常角化。已有数例单侧、线状、“带状疱疹样”或局限性损害的患者报道。我们报告3例符合哈普尔分类中1型嵌合型的局限性达里埃病病例,并复习关于达里埃病的遗传病因及“带状疱疹样”达里埃病的文献。