Literature DB >> 25098893

Update on ectodermal dysplasias clinical classification.

Nina Amália Brancia Pagnan1, Átila Fernando Visinoni.   

Abstract

Monogenic genetic disorders constitute a very large group of rare conditions, each of which is defined by a characteristic combination of phenotypic features. Their enormous clinical variability and their etiological heterogeneity may result in difficulties for the establishment of a syndromic diagnosis. In this context, classifications were proposed for different nosological groups, including ectodermal dysplasias. Freire-Maia proposed a clinical based classification, but nowadays the need of connecting clinical and molecular data on EDs demands a re-evaluation of the knowledge and the formulation of a new classification approach. The aim of this article is to provide an update of an article published in 2009 in this Journal. In order to check for new articles and information on ectodermal dysplasias, we have consulted the OMIM, PUBMED, and Science Direct online databases.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  clinical classification; ectodermal appendage alteration; ectodermal dysplasias

Mesh:

Year:  2014        PMID: 25098893     DOI: 10.1002/ajmg.a.36616

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  11 in total

Review 1.  Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Authors:  John Timothy Wright; Mary Fete; Holm Schneider; Madelaine Zinser; Maranke I Koster; Angus J Clarke; Smail Hadj-Rabia; Gianluca Tadini; Nina Pagnan; Atila F Visinoni; Birgitta Bergendal; Becky Abbott; Timothy Fete; Clark Stanford; Clayton Butcher; Rena N D'Souza; Virginia P Sybert; Maria I Morasso
Journal:  Am J Med Genet A       Date:  2019-01-31       Impact factor: 2.802

2.  Defective NaCl Reabsorption in Salivary Glands of Eda-Null X-LHED Mice.

Authors:  T Mukaibo; T Munemasa; C Masaki; C Y Cui; J E Melvin
Journal:  J Dent Res       Date:  2018-06-18       Impact factor: 6.116

3.  KDF1, encoding keratinocyte differentiation factor 1, is mutated in a multigenerational family with ectodermal dysplasia.

Authors:  Hanan E Shamseldin; Ola Khalifa; Yousef M Binamer; Abdulmonem Almutawa; Stefan T Arold; Hamad Zaidan; Fowzan S Alkuraya
Journal:  Hum Genet       Date:  2016-11-12       Impact factor: 4.132

4.  Clinical features, surgical outcomes and genetic analysis of ectodermal dysplasia with ocular diseases.

Authors:  Xi Chen; Wei-Xuan Zeng; Bao-Ying Duan; Yan-Yan Lin; Jia Liu; Zong-Duan Zhang
Journal:  Int J Ophthalmol       Date:  2022-07-18       Impact factor: 1.645

5.  Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.

Authors:  Eman A Rabie; Inas S M Sayed; Khalda Amr; Hoda A Ahmed; Mostafa I Mostafa; Nehal F Hassib; Heba El-Sayed; Suher K Zada; Ghada El-Kamah
Journal:  Genes (Basel)       Date:  2022-06-13       Impact factor: 4.141

6.  Genetic diagnosis for X-linked hypohidrotic ectodermal dysplasia family with a novel Ectodysplasin A gene mutation.

Authors:  Xin Ma; Xue Lv; Hong-Yan Liu; Xing Wu; Li Wang; Hao Li; Hai-Yan Chou
Journal:  J Clin Lab Anal       Date:  2018-07-13       Impact factor: 2.352

7.  Thermoregulation in Ectodermal Dysplasia: A Case Series.

Authors:  Heather Massey; James House; Michael Tipton
Journal:  Int J Environ Res Public Health       Date:  2019-11-15       Impact factor: 3.390

8.  Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.

Authors:  Binghui Zeng; Xue Xiao; Sijie Li; Hui Lu; Jiaxuan Lu; Ling Zhu; Dongsheng Yu; Wei Zhao
Journal:  Genes (Basel)       Date:  2016-09-19       Impact factor: 4.096

9.  Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.

Authors:  Binghui Zeng; Qi Zhao; Sijie Li; Hui Lu; Jiaxuan Lu; Lan Ma; Wei Zhao; Dongsheng Yu
Journal:  Genes (Basel)       Date:  2017-10-05       Impact factor: 4.096

10.  Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.

Authors:  Hoda A Ahmed; Ghada Y El-Kamah; Eman Rabie; Mostafa I Mostafa; Maha R Abouzaid; Nehal F Hassib; Mennat I Mehrez; Mohamed A Abdel-Kader; Yasmine H Mohsen; Suher K Zada; Khalda S Amr; Inas S M Sayed
Journal:  Genes (Basel)       Date:  2021-09-08       Impact factor: 4.096

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