<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>42</Volume>
      <Issue>10</Issue>
      <PubDate PubStatus="epublish">
        <Year>2013</Year>
        <Month>10</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Myelodysplastic Syndrome with 6q Deletion as the Sole Chromosome Abnormality in an Iranian Patient: A Case Report with Review of Literature</title>
    <FirstPage>1187</FirstPage>
    <LastPage>1191</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Shirin</FirstName>
        <LastName>Ferdowsi</LastName>
        <affiliation locale="en_US">1. Dept. of Hematology, Iranian Blood Transfusion Organization , Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Shirkoohi</LastName>
        <affiliation locale="en_US">2. Dept. of Molecular Genetics, Cancer Research Center, Cancer Institute, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences , Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Toogeh</LastName>
        <affiliation locale="en_US">3. Dept. of Hematology-Oncology and BMT Research Center, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences , Tehran, Iran.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The myelodysplastic syndrome (MDS) is a highly heterogenous disorder and karyotype analysis is helpful for diagnostic and prognostic estimation. Deletion in long arm chromosome 6 (6q del) as a sole abnormality is a rare event in MDS. This is the first case report of del (6q) as the only observed diagnostic change in Iran. We also reviewed the literature of this cytogenetic lesion.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/4376</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/4376/4025</pdf_url>
  </Article>
</Articles>
