An unusual manifestation of X-linked hypohidrotic ectodermal dysplasia with palmoplantar keratoderma

被引：1
作者：
De Brito, M. [1 ]
Ferguson, L. [1 ]
Mansour, S. [2 ]
Khan, I. [1 ]
机构：
[1] St Georges Healthcare NHS Trust, Dept Dermatol, London, England
[2] St Georges Univ London, St Georges Healthcare NHS Trust, London, England
来源：
CLINICAL AND EXPERIMENTAL DERMATOLOGY | 2020年 / 45卷 / 03期
关键词：
FAMILY;
D O I：
10.1111/ced.14096
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：352 / 353
页数：2
相关论文
共 5 条
  • [1] Kothiwala Sunil K, 2016, Indian Dermatol Online J, V7, P393
  • [2] Novel missense mutation in the EDA1 gene identified in a family with hypohidrotic ectodermal dysplasia
    Pozo-Molina, Glustein
    Reyes-Reali, Julia
    Mendoza-Ramos, Maria Isabel
    Villalobos-Molina, Rafael
    Garrido-Guerrero, Efrain
    Mendez-Cruz, Adolfo Rene
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54 (07) : 790 - 794
  • [3] Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A
    Schneider, P
    Street, SL
    Gaide, O
    Hertig, S
    Tardivel, A
    Tschopp, J
    Runkel, L
    Alevizopoulos, K
    Ferguson, BM
    Zonana, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) : 18819 - 18827
  • [4] Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway
    Wright, John Timothy
    Fete, Mary
    Schneider, Holm
    Zinser, Madelaine
    Koster, Maranke I.
    Clarke, Angus J.
    Hadj-Rabia, Smail
    Tadini, Gianluca
    Pagnan, Nina
    Visinoni, Atila F.
    Bergendal, Birgitta
    Abbott, Becky
    Fete, Timothy
    Stanford, Clark
    Butcher, Clayton
    D'Souza, Rena N.
    Sybert, Virginia P.
    Morasso, Maria I.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (03) : 442 - 447
  • [5] Wright JT, 2017, GENEREVIEWS
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