<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>44</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="epublish">
        <Year>2006</Year>
        <Month>08</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">"HYPEREOSINOPHILIC SYNDROME: REPORT OF A CASE AND REVIEW OF LITERATURE "</title>
    <FirstPage>285</FirstPage>
    <LastPage>287</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>H. Moayeri  Z. Oloomi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Idiopathic hypereosinophilic syndrome represents a heterogeneous group of leukoprolifrative disorders associated with prolonged eosinophilia of an undetectable cause with multi organ system dysfunction. It is a rare group disorder in children, most cases are reported in adult age group. We report a child with this syndrome who along with the usual features of the syndrome also had the presentation of cardiac and neurologic complications which did not respond to treatment.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/3201</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/3201/3179</pdf_url>
  </Article>
</Articles>
