Document Detail


Klippel-Trénaunay syndrome associated with great saphenous vein aplasia.
MedLine Citation:
PMID:  20118344     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
J Herman; D Musil
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Phlebology / Venous Forum of the Royal Society of Medicine     Volume:  25     ISSN:  1758-1125     ISO Abbreviation:  Phlebology     Publication Date:  2010 Feb 
Date Detail:
Created Date:  2010-02-01     Completed Date:  2010-04-15     Revised Date:  2010-12-10    
Medline Journal Info:
Nlm Unique ID:  9012921     Medline TA:  Phlebology     Country:  England    
Other Details:
Languages:  eng     Pagination:  35-7     Citation Subset:  IM    
Affiliation:
2nd Dept. of Surgery, Teaching Hospital-Medical Faculty, Palacký University, I.P. Pavlova 6, 775 20 Olomouc, Czech Republic. hermanjiricz@yahoo.co.uk
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MeSH Terms
Descriptor/Qualifier:
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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