April 08-09,2020 Sydney, Australia
13th International Conference on Genomics and Molecular Biology
May 25-26, 2020 Rome, Italy
Klippel Trenaunay syndrome is a rare congenital medical condition in which blood vessels or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb.
An average of 49 members are effected every year in Germany.
Sclerotherapy is a treatment for specific veins and vascular malformations in the affected area. It involves the injection of a chemical into the abnormal veins to cause thickening and obstruction of the targeted vessels. Such treatment may allow normal blood flow to resume. The greatest issue with KTS syndrome is that the blood flow and/or lymph flow may be impeded, and will pool in the affected area.