Lucker G P, Steijlen P M
Department of Dermatology, University Hospital, Nijmegen, The Netherlands.
Clin Exp Dermatol. 1995 May;20(3):226-9. doi: 10.1111/j.1365-2230.1995.tb01307.x.
Pachyonychia congenita is a distinct hereditary disorder of keratinization, in which dystrophy of all nails is associated with palmoplantar keratoderma and other hyperkeratoses. Recently a late-onset type has been reported. We report a second family with late-onset pachyonychia congenita, showing a remarkable clinical heterogeneity. Furthermore, one patient demonstrated a number of associated hyperkeratoses not previously recognized. Acitretin proved useful in the treatment of this late-onset form of pachyonychia congenita.
先天性厚甲症是一种独特的角化遗传性疾病,所有指甲的营养不良与掌跖角化病和其他角化过度相关。最近报道了一种迟发型。我们报告了第二个迟发性先天性厚甲症家族,表现出显著的临床异质性。此外,一名患者出现了一些以前未被认识到的相关角化过度。阿维A被证明对治疗这种迟发性先天性厚甲症有效。