Literature DB >> 14708603

Clouston syndrome can mimic pachyonychia congenita.

Maurice A M van Steensel1, Marcel F Jonkman, Michel van Geel, Peter M Steijlen, W H Irwin McLean, Frances J D Smith.   

Abstract

We studied three families suffering from nail abnormalities who had previously been diagnosed as pachyonychia congenita. No keratin gene mutations were detected. Sequencing of connexin 30 (GJB6 gene) in these patients identified heterozygous missense mutations G11R and A88V that are known to be associated with Clouston syndrome. This unexpected finding expands the Clouston syndrome phenotype and suggests that some patients diagnosed with pachyonychia may in fact be suffering from Clouston syndrome.

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Year:  2003        PMID: 14708603     DOI: 10.1046/j.1523-1747.2003.12527.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  3 in total

Review 1.  Connexins and pannexins in the integumentary system: the skin and appendages.

Authors:  Chrysovalantou Faniku; Catherine S Wright; Patricia E Martin
Journal:  Cell Mol Life Sci       Date:  2015-06-20       Impact factor: 9.261

2.  The molecular genetic analysis of the expanding pachyonychia congenita case collection.

Authors:  N J Wilson; E A O'Toole; L M Milstone; C D Hansen; A A Shepherd; E Al-Asadi; M E Schwartz; W H I McLean; E Sprecher; F J D Smith
Journal:  Br J Dermatol       Date:  2014-08-06       Impact factor: 9.302

3.  GJB6 mutation A88V for hidrotic ectodermal dysplasia in a Chinese family.

Authors:  Xiaofeng Shi; Dongya Li; Min Chen; Yichen Liu; Qi Yan; Xianqiu Yu; Yan Zhu; Yumei Li
Journal:  Int J Dermatol       Date:  2019-01-08       Impact factor: 2.736

  3 in total

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