Klippel-Trenaunay-Weber Syndrome [Klippelova-Trenaunayova nemoc]
- Terms
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angioosteohypertrofický syndrom
Klippelova-Trenaunayova choroba
Klippelova-Trénaunayova choroba
Klippelova-Trénaunayova nemoc
Klippelův-Trenaunayův syndrom
Klippelův-Trénaunayův syndrom
Klippelův-Trénaunayův-Weberův syndrom
parciální angiektatický gigantismus
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Angio-Osteohypertrophy Syndrome
Angioosteohypertrophy Syndrome
Congenital Dysplastic Angiopathy
Klippel Trenaunay Syndrome
Klippel-Trenaunay Disease
Klippel-Trenaunay Syndrome
Klippel-Trénaunay-Weber Syndrome
KTW 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.
- DUI
- D007715 MeSH Browser
- CUI
- M0012064
- History note
- 94; was KLIPPEL-TRENAUNAY DISEASE 1975-93 (see under ANGIOMATOSIS 1975-90)
- Online note
- use KLIPPEL-TRENAUNAY-WEBER SYNDROME to search KLIPPEL-TRENAUNAY DISEASE 1975-93; search ANGIOMATOSIS 1966-74
- Public note
- 94; was KLIPPEL-TRENAUNAY DISEASE 1975-93 (see under ANGIOMATOSIS 1975-90)
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