Document Detail


Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
MedLine Citation:
PMID:  19951641     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant genodermatosis that prominently occurs among Japanese and Korean individuals. Dyschromatosis symmetrica hereditaria presents with a mixture of hyperpigmented and hypopigmented macules distributed on the face and the dorsal aspects of the extremities. We report a case of a 4-year-old girl with DSH and review the pertinent features of this genodermatosis.
Authors:
Iman Hemmati; Joseph Lam
Publication Detail:
Type:  Case Reports; Journal Article     Date:  2009-11-15
Journal Detail:
Title:  Dermatology online journal     Volume:  15     ISSN:  1087-2108     ISO Abbreviation:  Dermatol. Online J.     Publication Date:  2009  
Date Detail:
Created Date:  2009-12-02     Completed Date:  2010-02-23     Revised Date:  2010-03-12    
Medline Journal Info:
Nlm Unique ID:  9610776     Medline TA:  Dermatol Online J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  5     Citation Subset:  IM    
Affiliation:
Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Female
Follow-Up Studies
Foot Dermatoses / diagnosis,  genetics
Genetic Predisposition to Disease*
Hand Dermatoses / diagnosis,  genetics
Humans
Hyperpigmentation / diagnosis,  genetics*
Hypopigmentation / diagnosis,  genetics*
Pedigree
Pigmentation Disorders / diagnosis,  genetics
Skin Diseases, Genetic / diagnosis*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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