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
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| Concept/Terms |
Klippel-Trenaunay-Weber Syndrome- Klippel-Trenaunay-Weber Syndrome
- Klippel Trenaunay Weber Syndrome
- Syndrome, Klippel-Trenaunay-Weber
- Angioosteohypertrophy Syndrome
- Angioosteohypertrophy Syndromes
- Syndrome, Angioosteohypertrophy
- Syndromes, Angioosteohypertrophy
- Congenital Dysplastic Angiopathy
- Angiopathies, Congenital Dysplastic
- Angiopathy, Congenital Dysplastic
- Congenital Dysplastic Angiopathies
- Dysplastic Angiopathies, Congenital
- Dysplastic Angiopathy, Congenital
- 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
- KTW Syndrome
- KTW Syndromes
- Syndrome, KTW
- Syndromes, KTW
- Angio-Osteohypertrophy Syndrome
- Angio Osteohypertrophy Syndrome
- Angio-Osteohypertrophy Syndromes
- Syndrome, Angio-Osteohypertrophy
- Syndromes, Angio-Osteohypertrophy
- Klippel-Trenaunay Disease
- Disease, Klippel-Trenaunay
- Klippel Trenaunay Disease
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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".
This graph shows the total number of publications written about "Klippel-Trenaunay-Weber Syndrome" by people in this website by year, and whether "Klippel-Trenaunay-Weber Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Klippel-Trenaunay-Weber Syndrome" by people in Profiles.
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Shields CL, Di Nicola M, Pellegrini M, Shields JA. CHOROIDAL MELANOMA IN PHAKOMATOSIS PIGMENTOVASCULARIS WITH KLIPPEL-TRENAUNAY SYNDROME. Retina. 2018 Nov; 38(11):2220-2227.
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Manquez ME, Shields CL, Demirci H, Shields JA, Beer P, Peters G. Choroidal melanoma in a teenager with Klippel-Tr?naunay-Weber syndrome. J Pediatr Ophthalmol Strabismus. 2006 Jul-Aug; 43(4):197-8.