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
- 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
|
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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Klippel-Trenaunay-Weber Syndrome" by people in Profiles.
-
Initial Experience With Propranolol Treatment of Lymphatic Anomalies: A Case Series. Pediatrics. 2016 09; 138(3).
-
Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. J Pediatr. 2015 Apr; 166(4):1048-54.e1-5.
-
Diverse manifestations and management options in Klippel-Trenaunay syndrome: a single centre 10-year experience. J Plast Surg Hand Surg. 2013 Sep; 47(4):303-7.
-
Renal agenesis in a child with ipsilateral hemihypertrophy. Pediatr Nephrol. 2010 Sep; 25(9):1751-4.
-
Endovascular radiofrequency ablation: a novel treatment of venous insufficiency in Klippel-Trenaunay patients. J Vasc Surg. 2008 Jun; 47(6):1339-45.
-
Extradural thoracic arteriovenous malformation in a patient with Klippel-Trenaunay-Weber syndrome: case report. Neurosurgery. 2002 Nov; 51(5):1275-8; discussion 1278-9.
-
Direct MR venography of persistent sciatic vein in a patient with Klippel-Trenaunay-Weber syndrome. AJR Am J Roentgenol. 2002 Feb; 178(2):513-4.