Dermoscopic features in a case of dyschromatosis symmetrica hereditaria
Author:
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2010.01110.x/fullpdf
Reference13 articles.
1. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003
2. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes;Kondo;J Dermatol,2008
3. Mutation analysis of the ADAR1 Gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis;Suzuki;J Invest Dermatol,2005
4. Mutation analysis of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene;Murata;J Dermatol Sci,2010
5. Using dermoscopic criteria and patient-related factors for the management of pigmented melanocytic nevi;Zalaudek;Arch Dermatol,2009
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3. Dermoscopic patterns of dyschromatosis universalis hereditaria with acral involvement;Clinical and Experimental Dermatology;2023-07-04
4. A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency;Clinical, Cosmetic and Investigational Dermatology;2023-04
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