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Clouston syndrome can mimic pachyonychia congenita.

Authors :
Steensel, M.A.M. van
Jonkman, M.F.
Geel, M. van
Steijlen, P.M.
McLean, W.H.I.
Smith, F.J.D.
Steensel, M.A.M. van
Jonkman, M.F.
Geel, M. van
Steijlen, P.M.
McLean, W.H.I.
Smith, F.J.D.
Source :
Journal of Investigative Dermatology; 1035; 1038; 0022-202X; 5; 121; ~Journal of Investigative Dermatology~1035~1038~~~0022-202X~5~121~~
Publication Year :
2003

Abstract

Contains fulltext : 184980.pdf (publisher's version ) (Closed access)<br />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.

Details

Database :
OAIster
Journal :
Journal of Investigative Dermatology; 1035; 1038; 0022-202X; 5; 121; ~Journal of Investigative Dermatology~1035~1038~~~0022-202X~5~121~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284127965
Document Type :
Electronic Resource