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<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>47</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Cerebral Vein Thrombosis: Screening of Acquired and Hereditary Thrombophilic Risk Factors</title>
    <FirstPage>197</FirstPage>
    <LastPage>202</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Payam</FirstName>
        <LastName>Sarraf</LastName>
        <affiliation locale="en_US">Department of Neurology, Imam Khomeiny Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>Ghaffarpoor</LastName>
        <affiliation locale="en_US">Department of Neurology, Imam Khomeiny Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hosein</FirstName>
        <LastName>Poormahmoodian</LastName>
        <affiliation locale="en_US">Department of Neurology, Imam Khomeiny Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hosein</FirstName>
        <LastName>Harrirchian</LastName>
        <affiliation locale="en_US">Department of Neurology, Imam Khomeiny Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Hasan</FirstName>
        <LastName>Hashemi</LastName>
        <affiliation locale="en_US">Department of Radiology, Imam Khomeiny Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Cerebral vein thrombosis (CVT) is an infrequent condition with a large variety of causes that can lead to serious disabilities. However, in 20% to 35% of cases, no cause is found. In this study we evaluated the hereditary (P &amp; C Proteins, antithrombin, mutation of prothrombin G20210A and factor V Leiden), other risk factors (hyperhomocycteinemia, factor VIII, ACL-ab, APL-ab, and OCP) and clinical manifestations among a population of Iranian patients with CVT. 18 women and 10 men aged 16 to 50 years with CVT were screened for inherited and acquired coagulation risk factors. No one had an abnormal ACL-ab, APL-ab or antithrombin III deficiency. One had prothrombin G20210A mutation (heterozygot) (3.6%). Hyperhomocycteinemia was observed in 5 patients (17.9%). APC-R was decreased in 3 (10.7%). 2 had positive factor V Leiden mutation (heterozygot) (7.1%). 17 had an increased of factor VIII (60.7). PS and PC deficiencies were each detected in two cases (7.1%). Conclusion: Our study suggests that screening for inherited thrombophilia may be an integral part in the diagnostic workup and duration of treatment in patients with CVT.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/3575</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/3575/3551</pdf_url>
  </Article>
</Articles>
