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Klippel-Trenaunay-Weber Syndrome

Known as: Syndrome, Klippel-Trénaunay-Weber, syndrome webers, Angio-Osteohypertrophy Syndrome 
A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and… 
National Institutes of Health

Papers overview

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2001
2001
There are many documented cases of Klippel-Trenaunay-Weber syndrome characterized by the triad of port wine stain, varicose veins… 
Highly Cited
1998
Highly Cited
1998
The Klippel–Trenaunay–Weber syndrome (KTWS) is generally thought to occur sporadically, following a somatic mutation model… 
Review
1997
Review
1997
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue… 
1996
1996
Klippel-Trénaunay-Weber syndrome is a rare congenital deep-vein malformation. Pregnancy in patients with this syndrome is rare… 
Review
1994
Review
1994
Klippel-Trenaunay-Weber syndrome is characterized by limb hypertrophy, varicose veins, and vascular nevus. The orofacial… 
1991
1991
A man with Klippel-Trenaunay-Weber syndrome had worsening pulmonary hypertension secondary to recurrent multiple pulmonary… 
1987
1987
The Klippel-Trenaunay-Weber syndrome consists of cutaneous port wine hemangiomas, superficial venous varicosities, and soft… 
Review
1978
Review
1978
Klippel-Trenaunay syndrome (KTS) is characterized by port-wine hemangiomas, deep venous system abnormalities, superficial… 
Highly Cited
1967
Highly Cited
1967
Summary The antitumor activity of the copper(II) chelate of 3-ethoxy-2-oxobutyraldehyde bis(thiosemicarbazone), Cu(II)KTS…