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一个患有掌跖表皮松解性角化过度症的家庭。

A family with palmoplantar epidermolytic hyperkeratosis.

作者信息

Berth-Jones J, Hutchinson P E

出版信息

Clin Exp Dermatol. 1989 Jul;14(4):313-6. doi: 10.1111/j.1365-2230.1989.tb01991.x.

Abstract

Familial epidermolytic hyperkeratosis confined to the palms and soles was first characterized by Klaus and Weinstein in 1970. This entity has been the subject of only four subsequent reports. We report a family previously diagnosed as suffering from tylosis (Thost Unna syndrome), in which eleven members have been affected, and review the literature on this disease. It would seem possible that this entity may be more common than the sparse literature would indicate, and that other cases may currently be masquerading as tylosis.

摘要

局限于手掌和足底的家族性表皮松解性角化过度症于1970年由克劳斯和温斯坦首次描述。此后关于这个病症仅有四份报告。我们报告一个先前被诊断为患胼胝形成(托斯特 - 昂纳综合征)的家族,其中11名成员患病,并回顾了关于这种疾病的文献。看起来这种病症可能比现有少量文献所显示的更为常见,而且目前可能有其他病例被误诊为胼胝形成。

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