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
- 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 |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 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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Response to sirolimus in capillary lymphatic venous malformations and associated syndromes: Impact on symptomatology, quality of life, and radiographic response. Pediatr Blood Cancer. 2023 04; 70(4):e30215.
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Vascular Anomaly Syndromes in the ISSVA Classification System: Imaging Findings and Role of Interventional Radiology in Management. Radiographics. 2022 10; 42(6):1598-1620.
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An atypical case of Klippel-Tr?naunay syndrome presenting with crossed-bilateral limb hypertrophy and postaxial polydactyly: a case report. BMC Pediatr. 2019 04 06; 19(1):95.
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Surgical treatment of varicose veins and venous malformations in Klippel-Trenaunay syndrome. Phlebology. 2016 Apr; 31(3):209-15.
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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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Focal congenital lipoatrophy and vascular malformation: a mild form of inverse Klippel-Trenaunay syndrome? Eur J Med Genet. 2012 Dec; 55(12):705-7.
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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature. 2004 Feb 12; 427(6975):640-5.
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Relief of iliofemoral vein occlusion with the Palma bypass in a patient with Klippel Trenaunay syndrome. Ann Vasc Surg. 2003 Jul; 17(4):449-55.