主要表现为色素脱失、色素沉着及掌跖过度角化，具此三联症者72例（7．35％）。
The main manifestation was hypopigment, hyperpigment, and palmoplantar Hyperkeratosis. Triad cases happened in 72 patients (7.35%).
本文报告了一例罕见的遗传性掌跖皮肤角化病—遗传性残毁性角化瘤，并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。
This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.
本文报告了一例罕见的遗传性掌跖皮肤角化病—遗传性残毁性角化瘤，并与各种掌跖皮肤角化症、断肢症的鉴别进行了讨论。
This paper is reported a rare case of palmoplanter keratoma hereditaria-keratoma hereditaria mutilans and differential diagnosis with various palmoplantar keratodermas and dactylolysis are discussed.
应用推荐