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Piebaldism: A brief report and review of the literature.
MedLine Citation:
PMID:  23130293     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Piebaldism is a rare autosomal dominant disorder of melanocyte development characterized by a congenital white forelock and multiple symmetrical stable hypopigmented or depigmented macules. We report a family with piebaldism affecting three successive generations and also review the literature.
Authors:
Saurabh Agarwal; Amit Ojha
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian dermatology online journal     Volume:  3     ISSN:  2249-5673     ISO Abbreviation:  Indian Dermatol Online J     Publication Date:  2012 May 
Date Detail:
Created Date:  2012-11-06     Completed Date:  2012-11-07     Revised Date:  2013-05-30    
Medline Journal Info:
Nlm Unique ID:  101586880     Medline TA:  Indian Dermatol Online J     Country:  India    
Other Details:
Languages:  eng     Pagination:  144-7     Citation Subset:  -    
Affiliation:
Department of Skin and VD, Government Medical College, Haldwani (Nainital), Uttarakhand, India.
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