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- W2155341606 abstract "Abstract Hereditary Angioedema is a hereditary disease caused by deficiency or loss of C1 i nhibitor (C1-INH), with an autosomal dominant inheritance pattern and which may be potentially life threatening. The prevalence of the disease is considerably low. In this case report, a 31 years old woman who has applied to the hospital with an angioedema attack after odontotherapy and who had angioedema attacks for many years with abdominal symptoms in the forefront and as a consequence to whom laparotomy was applied 3 times, is discussed together with literature. Hereditary Angioedema must certainly be considered for patients who apply to hospital with localized angioedema and especially with symptoms relating to upper airway tract and treatment strategy must be determined urgently, because delay in treatment increases morbidity and affects life quality. Keywords: Hereditary, angioedema, type ΙΙ Ozet Herediter Anjioodem, C1 Inhibitor (C1-INH) fonksiyon kaybi veya eksikligi ile ortaya cikan, otozomal dominant gecisli ve potansiyel olarak yasami tehdit edebilen kalitsal bir hastaliktir. Hastaligin prevelansi oldukca dusuktur. Bu olgu sunumunda uzun yillardir abdominal semptomlarin on planda oldugu, anjioodem ataklari geciren ve bu nedenle 3 kez laparotomi uygulanan, dis tedavisi sonrasi anjioodem atagi ile basvuran 31 yasinda kadin hasta literatur esliginde tartisildi. Lokalize anjioodemle ve ozellikle ust havayolunu ilgilendiren semptomlarla basvuran hastalarda herediter anjioodem mutlaka akilda bulundurulmali, acil tedavi stratejisi belirlenmelidir. Cunku tedavideki gecikme morbiditeyi arttirir ve yasam kalitesini olumsuz etkiler. Anahtar sozcukler: Herediter, anjioodem, t ip ΙΙ" @default.
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- W2155341606 date "2012-03-11" @default.
- W2155341606 modified "2023-09-27" @default.
- W2155341606 title "Hereditary angioedema type ΙΙ; report of a case" @default.
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- W2155341606 doi "https://doi.org/10.7197/cmj.v34i4.1008001427" @default.
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