Klippel-Trenaunay syndrome

The features of Klippel-Trenaunay-Weber syndrome are large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. The disorder resembles, clinically and in its lack of definite genetic basis, Sturge-Weber syndrome and indeed the two have been associated in some cases. Suggestions of a genetic 'cause' are meager.

1. Diseases of the lymphatic system
2. Congenital abnormalities

1. Sturge-Weber syndrome
2. Proteus syndrome

1. Syndrome