Document Detail

Marie Unna hereditary hypotrichosis.
MedLine Citation:
PMID:  10356404     Owner:  NLM     Status:  MEDLINE    
Hereditary congenital hypotrichosis is an autosomal dominant pilar dysplasia first described by Marie Unna in an extended German family. The diffuse hair defect typically occurs as an isolated phenomenon and the ultrastructural hair findings consist of both torsion and longitudinal grooving of the hair shaft. A large pedigree comprising 6 generations with 20 members affected by Marie Unna hypotrichosis from Italy is reported.
G Argenziano; E Sammarco; A Rossi; M Delfino; S Calvieri
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  European journal of dermatology : EJD     Volume:  9     ISSN:  1167-1122     ISO Abbreviation:  Eur J Dermatol     Publication Date:  1999 Jun 
Date Detail:
Created Date:  1999-08-24     Completed Date:  1999-08-24     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9206420     Medline TA:  Eur J Dermatol     Country:  FRANCE    
Other Details:
Languages:  eng     Pagination:  278-80     Citation Subset:  IM    
Department of Dermatology, Federico II University of Naples, via Pansini 5, 8013 Napoli, Italy.
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MeSH Terms
Hypotrichosis / congenital*,  genetics,  pathology

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

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