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Abstract Stroke occurs in 30.9 million individuals worldwide and is responsible for ~4 million deaths every year. In the United States, it is the third leading cause of death. The greatest burden of stroke, apart from death, is serious long-term physical and mental disability. Stroke survivors often experience physical handicap, depression, and cognitive dysfunction, which together affect their daily functioning, quality of life, and survival.(Giuseppe Mancia,2004) Stroke is the largest single cause of disability in the UK. While tests based upon biomarkers have been around for decades, interest in the applications of biomarkers has increased greatly in recent years. Biomarkers released into the blood stream following a stroke are useful not only for understanding the pathogenesis of stroke, but also play a significant role in the development of personalized medicine. The efficacy of current clinical models and imaging techniques for the diagnosis and prognosis of acute stroke could be improved when used in conjunction with blood biomarkers (Nazeeha Hasan et al,2012) The aim of this study is to explore the magnitude of (D dimer, Fibrinogen and C- reactive protein) within 24 hours as biomarkers of acute ischemic cerebral stroke and their relation to different ischemic stroke subtypes and their impact on the short term outcome after 30 days. |