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.
推出的年份: 1994
树号: C14.907.077.410
MeSH 单一 ID: D007715
进入的组:
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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