AI Summary & Key Takeaways
AI InsightWe present here 3 cases of KTWS whose diagnosis were made within the last three years at the neonatal period, at 18 month and at 3 years of age in our clinic of the Çukurova University, Medical Faculty, Balcali hospital and evaluated in the light of available literature on the KTWS.
📌 3 Key Takeaways
Abstract
The Klippel-Trenaunay-Weber Syndrome (KTWS) is a rare disorder in which the congenital vascular hamartomas, limb hypertrophy, cutaneous manifestation, lymphangiomas and atresia of lymph vessels with non-pitting edema. We present here 3 cases of KTWS whose diagnosis were made within the last three years at the neonatal period, at 18 month and at 3 years of age in our clinic of the Çukurova University, Medical Faculty, Balcali hospital and evaluated in the light of available literature on the KTWS.
Özet
Klippel-Trenaunay-Weber Sendromu (KTWS) şarap lekesi şeklinde hemanjiom, variköz venler ve yumuşak doku ve kemiklerde hipertrofi ile karakterize nadir bir sendromdur. Biz burada Çukurova Üniversitesi Tıp Fakültesi, Çocuk kliniğinde, son 3 yılda, yenidoğan, 18 aylıkken ve 3 yaşında iken tanı koyduğumuz Klippel-Trenaunay-Weber sendromlu 3 olgumuzu sunduk ve Klippel-Trenaunay-Weber sendromunu literatür ışığında gözden geçirdik.