Ectodermal Dysplasias: A Clinical and Molecular Review

被引:32
作者
Garcia-Martin, P. [1 ]
Hernandez-Martin, A. [1 ]
Torrelo, A. [1 ]
机构
[1] Hosp Infantil Nino Jesus, Servicio Dermatol, Madrid, Spain
来源
ACTAS DERMO-SIFILIOGRAFICAS | 2013年 / 104卷 / 06期
关键词
Genodermatosis; Ectodermal dysplasia; Nuclear Factor kappa B; Ectodysplasin; Protein p63;
D O I
10.1016/j.ad.2012.07.012
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The ectodermal dysplasias are a large group of hereditary disorders characterized by alterations of structures of ectodermal origin. Although some syndromes can have specific features, many of them share common clinical characteristics. Two main groups of ectodermal dysplasias can be distinguished. One group is characterized by aplasia or hypoplasia of ectodermal tissues, which fail to develop and differentiate because of a lack of reciprocal signaling between ectoderm and mesoderm, the other has palmoplantar keratoderma as its most striking feature, with additional manifestations when other highly specialized epithelia are also involved. In recent decades, the genes responsible for at least 30 different types of ectodermal dysplasia have been identified, throwing light on the pathogenic mechanisms involved and their correlation with clinical findings. (C) 2011 Elsevier Espana, S.L. and AEDV. All rights reserved.
引用
收藏
页码:451 / 470
页数:20
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