Document Detail


Dyschromatosis universalis hereditaria: A rare entity.
MedLine Citation:
PMID:  21810391     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Dyschromatosis universalis hereditaria is an infrequently occurring genodermatosis with peculiar pigmentary changes, consisting of varying sized, intermingled hyperpigmented and hypopigmented macules that give an overall impression of mottling. We hereby report a case of dyschromatosis universalis hereditaria in a young female with a family history of the disorder.
Authors:
Sumir Kumar; Bharat Bhushan Mahajan; Rajwinder Singh
Publication Detail:
Type:  Journal Article     Date:  2011-07-15
Journal Detail:
Title:  Dermatology online journal     Volume:  17     ISSN:  1087-2108     ISO Abbreviation:  Dermatol. Online J.     Publication Date:  2011  
Date Detail:
Created Date:  2011-08-03     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9610776     Medline TA:  Dermatol Online J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  6     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Venereology and Leprology, Guru Gobind Singh Medical College and Hospital, Faridkot, Punjab.
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