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Descriptor English: Klippel-Trenaunay-Weber Syndrome
Descriptor Spanish: Síndrome de Klippel-Trenaunay-Weber
Descriptor síndrome de Klippel-Trenaunay-Weber
Entry term(s) enfermedad de Klippel-Trenaunay
Scope note: Trastorno congénito caracterizado por la triada de malformaciones capilares (HEMANGIOMA), malformaciones venosas (FISTULA ARTERIOVENOSA) e hipertrofia de huesos y tejidos blandos en las extremidades. Este síndrome se debe a mutaciones en el gen VG5Q que codifica un potente estimulador de la angiogénesis.
Descriptor Portuguese: Síndrome de Klippel-Trenaunay-Weber
Descriptor French: Syndrome de Klippel-Trénaunay
Entry term(s): Angio Osteohypertrophy Syndrome
Angio-Osteohypertrophy Syndrome
Angio-Osteohypertrophy Syndromes
Angioosteohypertrophy Syndrome
Angioosteohypertrophy Syndromes
Angiopathies, Congenital Dysplastic
Angiopathy, Congenital Dysplastic
Congenital Dysplastic Angiopathies
Congenital Dysplastic Angiopathy
Disease, Klippel-Trenaunay
Dysplastic Angiopathies, Congenital
Dysplastic Angiopathy, Congenital
KTW Syndrome
KTW Syndromes
Klippel Trenaunay Disease
Klippel Trenaunay Syndrome
Klippel Trenaunay Weber Syndrome
Klippel Trénaunay Weber Syndrome
Klippel-Trenaunay Disease
Klippel-Trenaunay Syndrome
Klippel-Trenaunay Syndromes
Klippel-Trénaunay-Weber Syndrome
Syndrome, Angio-Osteohypertrophy
Syndrome, Angioosteohypertrophy
Syndrome, KTW
Syndrome, Klippel Trenaunay
Syndrome, Klippel-Trenaunay
Syndrome, Klippel-Trenaunay-Weber
Syndrome, Klippel-Trénaunay-Weber
Syndromes, Angio-Osteohypertrophy
Syndromes, Angioosteohypertrophy
Syndromes, KTW
Syndromes, Klippel-Trenaunay
Tree number(s): C14.907.077.410
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D007715
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH 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
History Note: 94; was KLIPPEL-TRENAUNAY DISEASE 1975-93 (see under ANGIOMATOSIS 1975-90)
DeCS ID: 31869
Unique ID: D007715
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
Klippel-Trenaunay-Weber Syndrome - Preferred
Concept UI M0012064
Scope note 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.
Preferred term Klippel-Trenaunay-Weber Syndrome
Entry term(s) Angio Osteohypertrophy Syndrome
Angio-Osteohypertrophy Syndrome
Angio-Osteohypertrophy Syndromes
Angioosteohypertrophy Syndrome
Angioosteohypertrophy Syndromes
Angiopathies, Congenital Dysplastic
Angiopathy, Congenital Dysplastic
Congenital Dysplastic Angiopathies
Congenital Dysplastic Angiopathy
Disease, Klippel-Trenaunay
Dysplastic Angiopathies, Congenital
Dysplastic Angiopathy, Congenital
KTW Syndrome
KTW Syndromes
Klippel Trenaunay Disease
Klippel Trenaunay Syndrome
Klippel Trenaunay Weber Syndrome
Klippel Trénaunay Weber Syndrome
Klippel-Trenaunay Disease
Klippel-Trenaunay Syndrome
Klippel-Trenaunay Syndromes
Klippel-Trénaunay-Weber Syndrome
Syndrome, Angio-Osteohypertrophy
Syndrome, Angioosteohypertrophy
Syndrome, KTW
Syndrome, Klippel Trenaunay
Syndrome, Klippel-Trenaunay
Syndrome, Klippel-Trenaunay-Weber
Syndrome, Klippel-Trénaunay-Weber
Syndromes, Angio-Osteohypertrophy
Syndromes, Angioosteohypertrophy
Syndromes, KTW
Syndromes, Klippel-Trenaunay



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