Document Detail


Photoletter to the editor: Dyschromatosis universalis hereditaria: an infrequently occurring entity in Europe.
MedLine Citation:
PMID:  23091589     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis mainly described in asian subjects. Here, we report a case of a caucasian 11-year-old boy with DUH and an unaffected twin brother. Parents were not consanguineous. A review of the main phenotical, clinical and hystological aspects of this rare entity is exhibited. Differential diagnose might be stablished with several pigmentary disorders, so Dermatologist might have this entity in mind to make a correct diagnose, specially in cases with no response to typical treatments.
Authors:
Nayra Merino de Paz; Marina Rodríguez-Martin; Patricia Contreras Ferrer; Maria Pestana-Eliche; Antonio Martin-Herrera; Antonio Noda-Cabrera
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of dermatological case reports     Volume:  6     ISSN:  1898-7249     ISO Abbreviation:  J Dermatol Case Rep     Publication Date:  2012 Sep 
Date Detail:
Created Date:  2012-10-23     Completed Date:  2012-10-24     Revised Date:  2013-05-30    
Medline Journal Info:
Nlm Unique ID:  101493700     Medline TA:  J Dermatol Case Rep     Country:  Poland    
Other Details:
Languages:  eng     Pagination:  96-7     Citation Subset:  -    
Affiliation:
Department of Dermatology, Hospital Universitario de Canarias, La Laguna, Tenerife, Spain.
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