 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
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| 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
- Klippel-Trénaunay-Weber Syndrome
- Klippel Trénaunay Weber Syndrome
- Syndrome, Klippel-Trénaunay-Weber
- Klippel-Trenaunay Disease
- Disease, Klippel-Trenaunay
- Klippel Trenaunay Disease
- Angioosteohypertrophy Syndrome
- Angioosteohypertrophy Syndromes
- Syndrome, Angioosteohypertrophy
- Syndromes, Angioosteohypertrophy
- Klippel Trenaunay Syndrome
- Syndrome, Klippel Trenaunay
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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.
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 |
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Below are the most recent publications written about "Klippel-Trenaunay-Weber Syndrome" by people in Profiles.
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Wu JK, Hooper ED, Laifer-Narin SL, Simpson LL, Kandel J, Shawber CJ. Initial Experience With Propranolol Treatment of Lymphatic Anomalies: A Case Series. Pediatrics. 2016 09; 138(3).
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Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovée JV, Rialon KL, Guevara CJ, Alomari AI, Greene AK, Fishman SJ, Kozakewich HP, Maclellan RA, Mulliken JB, Rahbar R, Spencer SA, Trenor CC, Upton J, Zurakowski D, Perkins JA, Kirsh A, Bennett JT, Dobyns WB, Kurek KC, Warman ML, McCarroll SA, Murillo R. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. J Pediatr. 2015 Apr; 166(4):1048-54.e1-5.
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Sreekar H, Dawre S, Petkar KS, Shetty RB, Lamba S, Naik S, Gupta AK. 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.
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Oren NC, Vurucu S, Karaman B, Ors F. Renal agenesis in a child with ipsilateral hemihypertrophy. Pediatr Nephrol. 2010 Sep; 25(9):1751-4.
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Frasier K, Giangola G, Rosen R, Ginat DT. Endovascular radiofrequency ablation: a novel treatment of venous insufficiency in Klippel-Trenaunay patients. J Vasc Surg. 2008 Jun; 47(6):1339-45.
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Alexander MJ, Grossi PM, Spetzler RF, McDougall CG. Extradural thoracic arteriovenous malformation in a patient with Klippel-Trenaunay-Weber syndrome: case report. Neurosurgery. 2002 Nov; 51(5):1275-8; discussion 1278-9.
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Peirce RM, Funaki B. 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.
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