Klippel-Trenaunay-Weber Syndrome
"Klippel-Trenaunay-Weber Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D007715
|
| MeSH Number(s) |
C14.907.077.410
|
| Concept/Terms |
Klippel-Trenaunay-Weber Syndrome- Klippel-Trenaunay-Weber Syndrome
- Klippel Trenaunay Weber Syndrome
- Syndrome, Klippel-Trenaunay-Weber
- Klippel Trenaunay Syndrome
- Syndrome, Klippel Trenaunay
- Klippel-Trenaunay Syndrome
- Klippel-Trenaunay Syndromes
- Syndrome, Klippel-Trenaunay
- Syndromes, Klippel-Trenaunay
- Klippel-Trénaunay-Weber Syndrome
- Klippel Trénaunay Weber Syndrome
- Syndrome, Klippel-Trénaunay-Weber
- Angioosteohypertrophy Syndrome
- Angioosteohypertrophy Syndromes
- Syndrome, Angioosteohypertrophy
- Syndromes, Angioosteohypertrophy
- Klippel-Trenaunay Disease
- Disease, Klippel-Trenaunay
- Klippel Trenaunay Disease
|
Below are MeSH descriptors whose meaning is more general than "Klippel-Trenaunay-Weber Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Klippel-Trenaunay-Weber Syndrome".
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Below are the most recent publications written about "Klippel-Trenaunay-Weber Syndrome" by people in Profiles.