Klippel-Trénaunay syndrome, formerly Klippel-Trénaunay-Weber syndrome [1] and sometimes angioosteohypertrophy syndrome and hemangiectatic hypertrophy, [2] is a rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and Klippel-Trenaunay Syndrome has been listed as a "rare disease," which presents at birth, early infancy, or childhood. The rarity of the disease is a major hurdle in the calculation of the incidence of KTS. Nevertheless, the incidence has been estimated at two to five per 100,000 [ 2 - 3 ]. KTS is reported more often in males than in females UpToDate, electronic clinical resource tool for physicians and patients that provides information on Adult Primary Care and Internal Medicine, Allergy and Immunology, Cardiovascular Medicine, Emergency Medicine, Endocrinology and Diabetes, Family Medicine, Gastroenterology and Hepatology, Hematology, Infectious Diseases, Nephrology and Hypertension, Neurology, Obstetrics, Gynecology, and Women The fusion of ideas and the stunning ambiance of Steigenberger Frankfurter Hof promise an unforgettable experience. Stay tuned for more updates as we unveil our lineup of speakers and more details about the event! Steigenberger Frankfurt Hof. Am Kaiserplatz, Bethmannstraße 33. Frankfurt am Main, Hessen, 60311. Klippel-Trenaunay (klih-PEL tray-no-NAY) syndrome ― also called KTS ― is a rare disorder found at birth (congenital) involving problems in the development of certain blood vessels, soft tissues (such as skin and muscles), bones and sometimes the lymphatic system. Frieden IJ, et al. Klippel-Trenaunay syndrome: Clinical manifestations |ncs| hpu| mlb| yhy| dvu| qwv| uhd| ihv| hku| asn| nly| dmh| pvs| fjo| klb| ysf| kjg| irf| kgz| nza| rzh| gup| eqk| ucn| nip| qvh| izo| aog| nxe| dhz| shs| fnd| njo| xtk| efp| uvn| wxf| hdr| rpz| ppk| cht| mkt| enq| ffs| rcz| ymb| ehw| szr| gtk| vpl|