@article{article_95755, title={A Newborn Case With Renal Vein Thrombosis Due to Double Mutations of Factor V Leiden and MTHFR}, journal={Çağdaş Tıp Dergisi}, volume={5}, pages={135–139}, year={2015}, DOI={10.16899/ctd.88818}, author={Altın, Hakan and Çitli, Şenol and Akçay, Ahmet}, keywords={Yenidoğan, Renal Ven Trombozu, Gen Mutasyonu}, abstract={<p>Newborns are more susceptible to thrombosis than adults due to their lower amount of anticoagulant and fibrinolytic system proteins.  Incidence of thrombosis rises with presence of the predisposing factors such as hypoxia , infection, dehydration, polycytemia, infants of diabetic mothers, intravenous catheter use, and prothrombotic genetic disorders. Renal vein thrombosis can lead to potentially serious health problems and clinically present with hematuria, renal failure, thrombocytopenia, hypertension, oliguria and palpable mass in the abdomen.  Although renal vein thrombosis is a rare disease of newborn its incidence has been increased in recent years. In this article we presented a newborn case with meconium aspiration syndrome and renal vein thrombosis with presence of the genetic predisposing factors as Factor V Leiden and MTHFR gene mutations. </p> <p>  </p>}, number={2}, publisher={Rabia YILMAZ}