Concept information
Preferred term
Klippel-Trenaunay-Weber Syndrome
Type
-
mesh:Descriptor
Definition
- A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.
Broader concept
Entry terms
- Angio-Osteohypertrophy Syndrome
- Angioosteohypertrophy Syndrome
- Congenital Dysplastic Angiopathy
- Klippel-Trenaunay Disease
- Klippel Trenaunay Syndrome
- Klippel-Trenaunay Syndrome
- Klippel-Trénaunay-Weber Syndrome
- KTW Syndrome
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Angiodysplasie ostéodystrophique de Klippel-Trénaunay
-
Maladie de Klippel-Trénaunay
-
Naevus variqueux ostéo-hypertrophique
-
Naevus variqueux ostéohypertrophique
-
Syndrome de Klippel-Trénaunay-Weber
URI
http://data.loterre.fr/ark:/67375/JVR-T8N0Q95X-G
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