Klippel-Trenaunay-Weber syndrome is a rare congenital syndrome characterized by capillary, venous or lymphatic malformation and hemihypertrophy. Only 1000 cases of this syndrome have been reported in the literature. A rare case of this syndrome is presented here, who presented with its visceral and vascular complications and was diagnosed for the first time.
Alan : Sağlık Bilimleri
Dergi Türü : Uluslararası
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