The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床病理现及家族史都符合
皮松解
角化症的诊断。
The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma.
临床病理现及家族史都符合
皮松解
角化症的诊断。
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、汗管瘤、睑黄瘤、良乳头状瘤、汗管角化症、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.
先天角化不良症(DKC)为一少见之
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.
本文报告了一例罕见的跖皮肤角化病—
残毁
角化瘤,并与各种
跖皮肤角化症、断肢症的鉴别进行了讨论。
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