Association of Prothrombin Gene Mutation with Sepsis in a Preterm with Multiple Intracardiac Thrombi

We report for the first time, a premature infant with multiple intracardiac thrombi and sepsis, who was heterozygous for the G20210A prothrombin gene variant. Anticoagulant treatment with low molecular weight heparin resulted in the complete disappearance of the thrombi. It may be suggested that pro...

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Veröffentlicht in:	Echocardiography (Mount Kisco, N.Y.) N.Y.), 2005-04, Vol.22 (4), p.340-344
Hauptverfasser:	Cinar, Asli, Dilber, Embiya, Karagoz, Tevfik, Bahadir, Nursat, Gucer, Safak, Tekinalp, Gulsevin, Gurgey, Aytemiz
Format:	Artikel
Sprache:	eng
Schlagworte:	Disease Progression Fatal Outcome Gene Expression Regulation Genetic Predisposition to Disease Heart Diseases - complications Heart Diseases - diagnostic imaging Heart Diseases - genetics Humans Infant, Newborn Infant, Premature intracardiac thrombi Male Mutation Polymorphism, Genetic prematurity Prothrombin - genetics prothrombin gene mutation Sepsis - complications Sepsis - diagnosis Severity of Illness Index Thromboembolism - complications Thromboembolism - diagnostic imaging Thromboembolism - genetics Ultrasonography
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