Turner sendromu, tipik fenotipik özellikler ve X kromozomunun sayısal veya yapısal anormallikleri ile karakterize genetik bir hastalıktır. Turner sendromlu hastalarda konjenital kalp hastalığı sıktır. En sık aortanın konjenital malformasyonları, biküspit aorta, aort koarktasyonu ve aort dilatasyonu görülür. Bilgimize göre, Turner sendromunda perikardiyal efüzyon yalnızca bir kez bildirilmiştir. Perikardiyal efüzyon saptanan 50 yaşında Turner sendromlu bir hasta sunuldu. Anahtar kelimeler: Turner sendromu, perikardiyal efüzyon, tamponat Abstract A patient with turner's syndrome associated with pericardial effusion causing cardiac tamponade: case report Turner syndrome is a genetic disorder characterized by certain phenotypic features and structural or numerical abnormalities of X chromosome. There is high prevalence of congenital heart defects in patients with Turner's syndrome. Aortic malformations, bicuspid aortic valve, coarctation of the aorta and aortic dilation are the most common defects. To the best of our knowledge, only one case of pericardial effusion with Turner's syndrome has been reported. A case of pericardial effusion in a 50-year-old patient with Turner's syndrome is presented. Key words: Turner's syndrome, pericardial effusion, tamponade
Turner syndrome is a genetic disease characterized by typical phenotypic characteristics and numerical or structural abnormalities of X chromosome. Congenital heart disease is common in patients with Turner syndrome. The most common is congenital malformations of the aorta, aorta, aorta coarctation and aorta dilatation. According to our information, pericardial fusion in Turner syndrome has been
Alan : Sağlık Bilimleri
Dergi Türü : Uluslararası
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