Literature DB >> 23407077

Nectinopathies: an emerging group of ectodermal dysplasia syndromes.

F Brancati1, E Agolini, P Fortugno.   

Abstract

Cleft Lip/Palate-Ectodermal Dysplasia and Ectodermal Dysplasia-Syndactyly Syndrome are rare congenital disorders caused by recessive mutations in the PVRL1 and PVRL4 genes, respectively. These genes encode nectins 1 and 4, an emerging class of molecules acting in cooperation with cadherins to form cell-cell adhesion especially at adherens junctions. Their role in skin, hair and teeth biology and in the fine-tuning morphogenesis of craniofacial (lip/palate) and limbs is yet to be outlined prompting future research. We propose refer to these entities (nectin 1-ED and nectin 4-ED) as "nectinopathies", which are likely to be underestimated/underdiagnosed ED syndomes.

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Year:  2013        PMID: 23407077

Source DB:  PubMed          Journal:  G Ital Dermatol Venereol        ISSN: 0392-0488            Impact factor:   2.011


  4 in total

Review 1.  Nectin family of cell-adhesion molecules: structural and molecular aspects of function and specificity.

Authors:  Dibyendu Samanta; Steven C Almo
Journal:  Cell Mol Life Sci       Date:  2014-10-19       Impact factor: 9.261

2.  Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation.

Authors:  Paola Fortugno; Emmanuelle Josselin; Konstantinos Tsiakas; Emanuele Agolini; Gianluca Cestra; Massimo Teson; René Santer; Daniele Castiglia; Giuseppe Novelli; Bruno Dallapiccola; Ingo Kurth; Marc Lopez; Giovanna Zambruno; Francesco Brancati
Journal:  J Invest Dermatol       Date:  2014-02-27       Impact factor: 8.551

3.  A Novel Missense Variant in the PVRL4 Gene Underlying Ectodermal Dysplasia-Syndactyly Syndrome in a Turkish Child.

Authors:  Leila Dardour; Katrien Cosyns; Koenraad Devriendt
Journal:  Mol Syndromol       Date:  2017-08-12

4.  Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review.

Authors:  Roberta Rotunno; Andrea Diociaiuti; Maria Lisa Dentici; Martina Rinelli; Michele Callea; Chiara Retrosi; Giovanna Zambruno; Emanuele Bellacchio; May El Hachem
Journal:  Genes (Basel)       Date:  2021-05-17       Impact factor: 4.096

  4 in total

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