| Klippel-Trenaunay-Weber syndrome. | |
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MedLine Citation:
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PMID: 9314616 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue hypertrophy of an extremity. Recognition is usually possible during infancy or early childhood, and evaluation and treatment is important because morbidity may be minimized. We will review the clinical features, etiology, assessment, and treatment of patients with Klippel-Trenaunay-Weber syndrome. |
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Authors:
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J G Meine; R A Schwartz; C K Janniger |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: Cutis; cutaneous medicine for the practitioner Volume: 60 ISSN: 0011-4162 ISO Abbreviation: Cutis Publication Date: 1997 Sep |
Date Detail:
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Created Date: 1997-11-06 Completed Date: 1997-11-06 Revised Date: 2009-11-11 |
Medline Journal Info:
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Nlm Unique ID: 0006440 Medline TA: Cutis Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 127-32 Citation Subset: IM |
Affiliation:
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New Jersey Medical School, Newark 07103-2714, USA. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Combined Modality Therapy Female Humans Infant Infant, Newborn Klippel-Trenaunay-Weber Syndrome / diagnosis*, physiopathology, therapy* Laser Therapy Male Prognosis |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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