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外胚层发育不良综合征中的出汗:综述

Sweating in ectodermal dysplasia syndromes. A review.

作者信息

Berg D, Weingold D H, Abson K G, Olsen E A

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC 27710.

出版信息

Arch Dermatol. 1990 Aug;126(8):1075-9.

PMID:2200347
Abstract

Ectodermal dysplasia syndromes are currently classified based on constellations of clinical features, a major one of which is the presence or absence of normal sweating. The evaluation of sweating in these disorders has not been performed in a standardized manner, as is shown here in this literature review of a sampling of ectodermal dysplasia syndromes. Accurate evaluation of sweating is important not only in enabling more effective diagnosis and classification of patients with these syndromes, but also in aiding genetic counseling by potential detection of carrier states. A review of the variety of sweat tests currently in use is presented.

摘要

外胚层发育异常综合征目前是根据一系列临床特征进行分类的,其中一个主要特征是有无正常出汗。如本文对外胚层发育异常综合征样本的文献综述所示,这些疾病中出汗情况的评估尚未以标准化方式进行。准确评估出汗情况不仅对于更有效地诊断和分类这些综合征患者很重要,而且有助于通过潜在检测携带者状态来进行遗传咨询。本文介绍了目前使用的各种汗液测试。

相似文献

1
Sweating in ectodermal dysplasia syndromes. A review.外胚层发育不良综合征中的出汗:综述
Arch Dermatol. 1990 Aug;126(8):1075-9.
2
Sweating in the 'anhidrotic type' of congenital ectodermal dysplasia.先天性外胚层发育不良“无汗型”的出汗情况
Dermatologica. 1975;150(5):277-82.
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[Hypohidrotic ectodermal dysplasia: A cause of fever of unknown origin].[少汗型外胚层发育不良:不明原因发热的一个病因]
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[Congenital ectodermal dysplasia].[先天性外胚层发育不良]
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Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes.外胚层发育不良,表现出AEC综合征、拉普-霍奇金综合征和CHAND综合征之间的临床重叠。
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Acetylcholine-induced activation of the eccrine sweat glands in a case of hypohidrotic congenital ectodermal dysplasia.乙酰胆碱诱导的少汗性先天性外胚层发育不良病例中汗腺的激活
J Electron Microsc (Tokyo). 1989;38(5):371-81.
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Dental and oral abnormalities in selected ectodermal dysplasia syndromes.
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Cardio-facio-cutaneous syndrome with hemihidrosis: ectodermal dysplasias spectrum?伴有半侧多汗的心脏-颜面-皮肤综合征:外胚层发育不良谱系?
Int J Dermatol. 2006 Dec;45(12):1481-2. doi: 10.1111/j.1365-4632.2006.03202.x.
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Oral rehabilitation of a patient with ectodermal dysplasia with prosthodontics treatment.一名外胚层发育不全患者的口腔修复与义齿修复治疗
Indian J Dermatol. 2013 May;58(3):241. doi: 10.4103/0019-5154.110851.
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An insight into the genesis of hypohidrotic ectodermal dysplasia in a case report.一例报告中对少汗型外胚层发育不良病因的深入剖析。
Case Rep Dent. 2012;2012:281074. doi: 10.1155/2012/281074. Epub 2012 Dec 18.
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Ocular and non-ocular manifestations of hypohidrotic ectodermal dysplasia.少汗型外胚层发育不良的眼部和非眼部表现。
BMJ Case Rep. 2011 Apr 1;2011:bcr0120113731. doi: 10.1136/bcr.01.2011.3731.
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Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity?少汗型外胚层发育不良、中枢神经系统畸形及独特面部特征:一种独特疾病实体的确认?
J Med Genet. 1993 Mar;30(3):245-7. doi: 10.1136/jmg.30.3.245.
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Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.X连锁低汗性外胚层发育不良家系中新生突变的检测及其起源分析。
J Med Genet. 1994 Apr;31(4):287-92. doi: 10.1136/jmg.31.4.287.