| Klippel-Trénaunay syndrome associated with great saphenous vein aplasia. | |
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MedLine Citation:
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PMID: 20118344 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Klippel-Trénaunay syndrome (KTS) is a rare, sporadic, congenital vascular disease of unknown aetiology. KTS could be associated with infliction of other regions. An association with great saphenous vein aplasia has never been described. |
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Authors:
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J Herman; D Musil |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Phlebology / Venous Forum of the Royal Society of Medicine Volume: 25 ISSN: 1758-1125 ISO Abbreviation: Phlebology Publication Date: 2010 Feb |
Date Detail:
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Created Date: 2010-02-01 Completed Date: 2010-04-15 Revised Date: 2010-12-10 |
Medline Journal Info:
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Nlm Unique ID: 9012921 Medline TA: Phlebology Country: England |
Other Details:
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Languages: eng Pagination: 35-7 Citation Subset: IM |
Affiliation:
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2nd Dept. of Surgery, Teaching Hospital-Medical Faculty, Palacký University, I.P. Pavlova 6, 775 20 Olomouc, Czech Republic. hermanjiricz@yahoo.co.uk |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adult Hamartoma / complications Humans Klippel-Trenaunay-Weber Syndrome / complications* Leg / blood supply*, radiography Magnetic Resonance Angiography Male Saphenous Vein / abnormalities* Skin Diseases / complications Stockings, Compression Varicose Veins / etiology, surgery |
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