<?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>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2006</Year>
        <Month>12</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">M&#xD6;EBIUS SYNDROME AND CORPUS CALLOSUM AGENESIS; A CASE REPORT</title>
    <FirstPage>432</FirstPage>
    <LastPage>434</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>M. R. Ashrafi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>I. Hussain  S. M. A. Zamani</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">Moebius Syndrome is a rare congenital disorder of the facial and abducens nerve. Other cranial nerves may be involved, such as V, IX and XII. Several central nervous system anomalies including hypoplastic or dysplastic brain stem, straightening of the fourth ventricle floor, focal necrosis and calcifications of cranial nerve nuclei have been reported in association with Moebius syndrome, but we report a 18 months old boy of moebius syndrome with corpus callosum agenesis that has not been reported yet.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/3231</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/3231/3209</pdf_url>
  </Article>
</Articles>
