Document Detail


Congenital absence of dermatoglyphs.
MedLine Citation:
PMID:  8340514     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital absence or unusual patterns of human dermatoglyphs (fingerprints) occur in several syndromes that are rare and poorly understood. The abnormalities of dermatoglyphs fall into four categories: complete absence, ridge hypoplasia, ridge dissociation, and ridges-off-the-end. Complete congenital absence of ridges is an exceedingly rare syndrome that consists of neonatal blisters and milia, adult traumatic blistering and fissuring, absence of sweating, contracture of digits, and absence of dermatoglyphs on the hands and feet. The syndrome is inherited in an autosomal dominant pattern, and only two kindreds have been described in the literature. We describe a newly identified patient and kindred with findings similar to the previously reported cases and review the clinical and histopathologic findings of this syndrome.
Authors:
M Límová; K L Blacker; P E LeBoit
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of the American Academy of Dermatology     Volume:  29     ISSN:  0190-9622     ISO Abbreviation:  J. Am. Acad. Dermatol.     Publication Date:  1993 Aug 
Date Detail:
Created Date:  1993-08-31     Completed Date:  1993-08-31     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  7907132     Medline TA:  J Am Acad Dermatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  355-8     Citation Subset:  IM    
Affiliation:
Department of Dermatology, University of California, San Francisco 94143-0316.
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MeSH Terms
Descriptor/Qualifier:
Adult
Biopsy
Congenital Abnormalities / genetics
Dermatoglyphics*
Female
Fingers
Humans
Microscopy, Electron
Pedigree
Skin / pathology
Skin Abnormalities*

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


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