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<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>45</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2016</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report</title>
    <FirstPage>376</FirstPage>
    <LastPage>380</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mohammad Yahya</FirstName>
        <LastName>VAHIDI MEHRJARDI</LastName>
        <affiliation locale="en_US">Medical Genetics Research Center, Shahid Sadoughi University of Medical  Sciences, Yazd, Iran AND Dept. of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoud</FirstName>
        <LastName>DEHGHAN TEZERJANI</LastName>
        <affiliation locale="en_US">Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahmoud</FirstName>
        <LastName>NORI-SHADKAM</LastName>
        <affiliation locale="en_US">Dept. of Pediatrics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Mehdi</FirstName>
        <LastName>KALANTAR</LastName>
        <affiliation locale="en_US">Dept. of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran	AND Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadreza</FirstName>
        <LastName>DEHGHANI</LastName>
        <affiliation locale="en_US">Medical Genetics Research Center, Shahid Sadoughi University of Medical  Sciences, Yazd, Iran AND Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The interpretation of supernumerary chromosome is important for genetic counseling and prognosis. Here, we used SNP array and conventional karyotyping method to identify a denovo marker chromosome originated from chromosome 22 and 11 in a newborn transferred to the Neonatal Intensive Care Unit of Shahid Sadoughi Hospital in 2015.&#xA0; Clinical abnormalities identified in the newborn were dysmorphic face, intrauterine growth retardation, atrial septal defect (ASD), the hypoplasia of corpus callosum and septum pellucidum. These clinical abnormalities can be related to this marker, and it may help genetic counselor for predicting abnormality risk in susceptible individuals as well as prenatal diagnosis.&#xA0;

&#xA0;</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/6271</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/6271/5334</pdf_url>
  </Article>
</Articles>
