Document Detail


Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
MedLine Citation:
PMID:  20609155     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature.
Authors:
Lindsey B Finklea; Melinda R Mohr; Molly M Warthan; David H Darrow; Judith V Williams
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Pediatric dermatology     Volume:  27     ISSN:  1525-1470     ISO Abbreviation:  Pediatr Dermatol     Publication Date:    2010 May-Jun
Date Detail:
Created Date:  2010-07-08     Completed Date:  2010-10-25     Revised Date:  2011-01-11    
Medline Journal Info:
Nlm Unique ID:  8406799     Medline TA:  Pediatr Dermatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  303-5     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
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MeSH Terms
Descriptor/Qualifier:
Humans
Infant
Infant, Newborn
Klippel-Trenaunay-Weber Syndrome / diagnosis*
Male
Neurocutaneous Syndromes / diagnosis*
Sturge-Weber Syndrome / diagnosis*
Vascular Malformations / diagnosis*

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


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