Benoldi D, Zucchi A, Allegra F
Istituto di Clinica Dermosifilopatica, Università di Parma, Italy.
Clin Exp Dermatol. 1993 May;18(3):261-2. doi: 10.1111/j.1365-2230.1993.tb02183.x.
A case of non-familial multiple digitate hyperkeratosis is reported. Digitate hyperkeratosis is a new, non-follicular disorder of keratinization and three different types have been distinguished in the literature: the familial type, with an autosomal dominant trait; the sporadic type; and the post-inflammatory type.
报告了一例非家族性多发性指状角化过度病例。指状角化过度是一种新的非毛囊性角化异常疾病，文献中已区分出三种不同类型：具有常染色体显性特征的家族型；散发型；以及炎症后型。
