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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
We present a Klippel-Trenaunay-Weber syndrome case with nonimmune hydrops fetalis
📌 3 Key Takeaways
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Objective & Hypothesis:Klippel-Trenaunay-Weber syndrome is characterized by cutaneous hemangiomas, varicosities and soft tissue and bone hypertrophy, and was first described by Klippel and Trenaunay in 1900.
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Key Findings & Data:Klippel-Trenaunay-Weber syndrome is characterized by cutaneous hemangiomas, varicosities and soft tissue and bone hypertrophy, and was first described by Klippel and Trenaunay in 1900.
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Conclusion & Impact:We present a Klippel-Trenaunay-Weber syndrome case with nonimmune hydrops fetalis
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Klippel-Trenaunay-Weber syndrome is characterized by cutaneous hemangiomas, varicosities and soft tissue and bone hypertrophy, and was first described by Klippel and Trenaunay in 1900. We present a Klippel-Trenaunay-Weber syndrome case with nonimmune hydrops fetalis
Özet
İlk defa Klippel ve Trenaunay tarafından 1900 yılında tanımlanan Klippel-Trenaunay-Weber sendromu kutanöz hemanjiyomatöz lezyonlar, varikozite ve yumuşak doku ve kemik deformitesi ile karakterize bir sendromdur. Burada nonimmün hidrops fetalisi olan bir Klippel-Trenaunay-Weber sendromu vakası sunulmuştur.
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Cite This Article
SATAR, M., ŞAŞMAZ, İ., YAPICIOĞLU, H., ÖZGÜNEN, T. F., NARLI, N. (2022). Klippel-Trenaunay-Weber syndrome with nonimmune hydrops fetalis: A case report. Çocuk Sağlığı ve Hastalıkları Dergisi, Cilt: 44 - Sayı: 2, 152–154. https://ajindex.com/articles/484181