Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis-A Case of Mistaken Identity and Review of the Literature
Author:
Affiliation:
1. Department of General Medical Education; San Antonio Military Medical Center; Fort Sam Houston Texas
2. Department of Dermatology; San Antonio Military Medical Center; Fort Sam Houston Texas
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12652/fullpdf
Reference17 articles.
1. Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria;Cui;PLoS One,2013
2. Infancy- and childhood-onset dyschromatoses;Vachiramon;Clin Exp Dermatol,2011
3. Mutations in ABCB6 cause dyschromatosis universalis hereditaria;Zhang;J Invest Dermatol,2013
4. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria;Liu;PLoS One,2014
5. Dyschromatosis universalis hereditaria: report of a case and review of the literature;Al Hawsawi;Pediatr Dermatol,2002
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