Rania Srag Eldin Sayed <br/><br/>
Association of factor V leiden and prothrombin gene mutations with thrombotic risk in patients with sickle cell anemia /  
 العلاقة بين التحور الجينى لعامل التجلط الخامس و البروثروبين و احتمال التجلط فى مرضى الانيميا المنجلية 
Rania Srag Eldin Sayed ; Supervised Mona Salah Eldin Hamdy , Heba Mahmoud Gouda , Iman Abdelmohsen Abdu Shaheen 
 - Cairo :   Rania Srag Eldin Sayed ,   2010 
 - 112P. :   charts , facsimiles ;   25cm 
<br/><br/>Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology 
<br/><br/> Sickle cell disease ( SCD ) is a group of genetic disorders of hemoglobin that causes multisystem morbidity and an increased risk of early death . Vascular complications are an important aspect of sick cell anemia although there is controversial evidence surrounding the role of thrombosis in the complication . Among the crucial inherited risk factors are factor V Leiden ( G1619A ) and prothrombin gene G20210A mutations 
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<br/><br/><label>Subjects--Index Terms: </label>Factor V Leiden Prothrombin gene mutation Sickle cell disease