Back to Search Start Over

An atypical form of dyskeratosis congenita with renal agenesis and no mutation in DKC1, TERC and TERT genes.

Authors :
Balci, S.
Engiz, O.
Erekul, A.
Gozdasoglu, S.
Vulliamy, T.
Source :
Journal of the European Academy of Dermatology & Venereology. May2009, Vol. 23 Issue 5, p607-608. 2p. 1 Color Photograph.
Publication Year :
2009

Abstract

A letter to the editor is presented which discusses a case study of a 19-year-old male patient who was diagnosed with dyskeratosis congenita (DC), an inherited disease which is characterized with abnormal skin pigmentation, mucosal leukoplakia, and nail dystrophy.

Subjects

Subjects :
*LETTERS to the editor

Details

Language :
English
ISSN :
09269959
Volume :
23
Issue :
5
Database :
Academic Search Index
Journal :
Journal of the European Academy of Dermatology & Venereology
Publication Type :
Academic Journal
Accession number :
37307431
Full Text :
https://doi.org/10.1111/j.1468-3083.2008.02985.x