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日本无汗/少汗性外胚层发育不良的流行病学调查:过敏性疾病高发。

An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases.

机构信息

Department of Dermatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Department of Dermatology, Yamaguchi University Graduate School of Medicine, Ube, Japan.

出版信息

J Dermatol. 2022 Apr;49(4):422-431. doi: 10.1111/1346-8138.16278. Epub 2021 Dec 13.

Abstract

Anhidrotic/hypohidrotic ectodermal dysplasia (A/HED) is a congenital disorder characterized by anhidrosis/hypohidrosis and inadequate hair and dental dysplasia. Large-scale case studies of patients with A/HED have already been conducted overseas, while there has been no large-scale study, but only a few case reports in Japan. Furthermore, an epidemiological study of this disease has not been conducted in Japan to date. The purpose of this study was to investigate the clinical characteristics of A/HED patients, the status of genetic aberrations and complications of A/HED in Japan. Initially, we conducted a physician-initiated questionnaire survey of A/HED patients who visited medical institutions across Japan to investigate their backgrounds, clinical symptoms, genotypes, diagnostic methods and complications of A/HED. We also investigated the presence or absence of various allergic diseases (atopic dermatitis-like skin manifestations, bronchial asthma and food allergies). Questionnaires were also obtained from 26 patients with ectodermal dysplasia (ED) who visited four medical institutions. We compared the incidence of allergic diseases in healthy controls in a similar study to that of patients. Twenty-four of those patients were considered to have A/HED, of which 18 had a confirmed genetic diagnosis and were genotyped. All patients had anhidrosis or hypohidrosis, hair and dental dysplasia, and unique facial appearance; 23 patients had several cutaneous manifestations and seven patients had periorbital pigmentation. In addition, there was a significantly higher incidence of atopic dermatitis-like cutaneous manifestations, bronchial asthma and food allergies in the A/HED patients than in healthy controls. We report the results from a questionnaire survey of 24 patients with A/HED. This is the first report of a large number of A/HED patients in Japan. This study clarifies the status of clinical diagnosis and genetic testing of A/HED patients in Japan, as well as the characteristics of their skin symptoms and allergic complications.

摘要

无汗/少汗性外胚层发育不良(A/HED)是一种先天性疾病,其特征为无汗/少汗以及毛发和牙齿发育不良。已经在海外对 A/HED 患者进行了大规模病例研究,但在日本,仅有少数病例报告,而没有大规模的研究。此外,迄今为止,日本尚未对该疾病进行流行病学研究。本研究旨在调查日本 A/HED 患者的临床特征、遗传异常状况和并发症。最初,我们对在日本各地医疗机构就诊的 A/HED 患者进行了医生发起的问卷调查,以调查他们的背景、临床症状、基因型、诊断方法和 A/HED 的并发症。我们还调查了各种过敏性疾病(特应性皮炎样皮肤表现、支气管哮喘和食物过敏)的存在情况。我们还从四家医疗机构就诊的 26 例外胚层发育不良(ED)患者那里获得了问卷。我们将类似研究中健康对照组的过敏性疾病发生率与患者进行了比较。其中 24 名患者被认为患有 A/HED,其中 18 名患者具有明确的基因诊断,并进行了基因分型。所有患者均存在无汗或少汗、毛发和牙齿发育不良以及独特的面部外观;23 名患者存在多种皮肤表现,7 名患者存在眶周色素沉着。此外,A/HED 患者的特应性皮炎样皮肤表现、支气管哮喘和食物过敏的发生率明显高于健康对照组。我们报告了对 24 名 A/HED 患者进行问卷调查的结果。这是日本首次报告大量 A/HED 患者。本研究阐明了日本 A/HED 患者的临床诊断和基因检测状况,以及其皮肤症状和过敏并发症的特征。

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