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