Klippel-Trenaunay-Weber Syndrome
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.
Year introduced: 1994
PubMed search builder options
Subheadings:
Tree Number(s): C14.907.077.410
MeSH Unique ID: D007715
Entry Terms:
- 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
- Angio-Osteohypertrophy Syndrome
- Angio Osteohypertrophy Syndrome
- Angio-Osteohypertrophy Syndromes
- Syndrome, Angio-Osteohypertrophy
- Syndromes, Angio-Osteohypertrophy
- 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
- Klippel-Trenaunay Disease
- Disease, Klippel-Trenaunay
- Klippel Trenaunay Disease