Sanderson Elisabeth A, Killoran Christina E, Pedvis-Leftick Anita, Wilkel Caroline S
Boston University School of Medicine, Boston, Massachusetts, USA.
J Dermatol. 2007 Nov;34(11):761-4. doi: 10.1111/j.1346-8138.2007.00379.x.
Darier's disease is a rare autosomal dominant genodermatosis. Characteristic skin and nail changes consist of bilateral crusted red-brown papules and plaques in a seborrheic distribution, and V-shaped nicking or longitudinal ridging of the nails. In limited cases, a segmental distribution of this disease may be present in which localized lesions, found along the lines of Blaschko, are otherwise indistinguishable from those of generalized Darier's disease. Genomic mosaicism in localized lesions of Darier's disease is a new concept that was recently demonstrated in individuals of mosaic phenotypes. Both type 1 and type 2 mosaic phenotypes have been reported. We report two cases of type 1 localized Darier's disease in a Blaschkoid distribution and review the genetic implications of phenotypic mosaicism within the field of Darier's disease.
达里埃病是一种罕见的常染色体显性遗传性皮肤病。其特征性的皮肤和指甲改变包括双侧结痂的红棕色丘疹和斑块,呈脂溢性分布,以及指甲的V形切迹或纵嵴。在少数情况下,该病可能呈节段性分布,即沿布拉斯科线出现的局限性损害,在其他方面与泛发性达里埃病的损害无法区分。达里埃病局限性损害中的基因组镶嵌现象是一个新概念,最近在具有镶嵌表型的个体中得到证实。1型和2型镶嵌表型均有报道。我们报告了两例呈布拉斯科样分布的1型局限性达里埃病病例,并综述了达里埃病领域内表型镶嵌现象的遗传学意义。