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肠病性肢端皮炎

Acrodermatitis enteropathica.

作者信息

Maverakis Emanual, Lynch Peter J, Fazel Nasim

机构信息

University of California, Davis Department of Dermatology, USA.

出版信息

Dermatol Online J. 2007 Jul 13;13(3):11.

Abstract

A 13-year-old girl presented with a history of red scaly plaques involving the chest, arms and legs beginning in infancy. Punch biopsy revealed psoriasiform hyperplasia and pallor of the epidermis. The patient's serum zinc level was 36 mug/dl [nl. 66-144 mug/dl]. A diagnosis of acrodermatitis enteropathica was established and the patient responded well to zinc replacement therapy. Acrodermatitis enteropathica is a rare autosomal recessive disorder caused by mutations in SLC39A4, which encodes the tissue-specific zinc transporter ZIP4.

摘要

一名13岁女孩自婴儿期起胸部、手臂和腿部出现红色鳞屑斑块。皮肤活检显示为银屑病样增生及表皮苍白。患者血清锌水平为36μg/dl[正常范围66 - 144μg/dl]。诊断为肠病性肢端皮炎,患者对补锌治疗反应良好。肠病性肢端皮炎是一种罕见的常染色体隐性疾病,由编码组织特异性锌转运蛋白ZIP4的SLC39A4基因突变引起。

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