The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床病理表现及家族史都符合掌蹠表皮松解角症的诊断。
The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床病理表现及家族史都符合掌蹠表皮松解角症的诊断。
Treatment: milium, syringgoma, xanthoma of eyelid, benignpapilloma, sudoriceratosis, facial explosive powder thesaurismosis,helosis, leucoderma, acne rosacea, and encapsulated acne,etc.
9、治疗:栗丘疹、汗管、睑黄、良乳头状、汗管角症、爆炸伤异物(爆炸粉粒沉着症)、鸡眼、胼底、白癜风、酒渣鼻、包裹粉刺等。
Dyskeratosis congenita (DKC) is a rare inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy, and mucosal leukoplakia.
先天角不良症(DKC)为一少见之遗传疾病,三项主要特徵为皮肤色素异常、 指甲生长异常及黏膜白斑症。
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.
本文报告了一罕见的遗传掌跖皮肤角病—遗传残毁角,与各种掌跖皮肤角症、断肢症的鉴别进行了讨论。
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