Kouloubis Nina, van der Velden Jaap J A J
Albert Schweitzer ziekenhuis, afd. Dermatologie, Dordrecht.
Ned Tijdschr Geneeskd. 2013;157(51):A7007.
A 22-year-old women visited the dermatologist with hypertrophic finger- and toenails, palmoplantar keratoderma and oral leukokeratosis since her childhood. The diagnosis 'pachyonychia congenita type 1' was made. This is a rare dermatosis with an autosomal dominant inheritance pattern. The treatment is symptomatic.
一名22岁女性自幼患有肥厚性手指甲和脚趾甲、掌跖角化病及口腔黏膜白斑，遂前往皮肤科就诊。诊断为1型先天性厚甲症。这是一种罕见的皮肤病，呈常染色体显性遗传模式。治疗以对症治疗为主。
