<?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>44</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Premature Craniosynostosis in a Rare Genetic Disease- A Case Report</title>
    <FirstPage>404</FirstPage>
    <LastPage>6</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Hasnain Abbas</FirstName>
        <LastName>Dharamshi</LastName>
        <affiliation locale="en_US">Karachi Medical and Dental College, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Tufail</FirstName>
        <LastName>Raza</LastName>
        <affiliation locale="en_US">Baqai Medical College, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Ali Abbas</FirstName>
        <LastName>Mohsin Ali</LastName>
        <affiliation locale="en_US">Sindh Medical College/Dow university of Health Sciences, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Zuhair</FirstName>
        <LastName>Lilani</LastName>
        <affiliation locale="en_US">Karachi Medical and Dental College, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Syed Zohaib</FirstName>
        <LastName>Ahsan</LastName>
        <affiliation locale="en_US">Sindh Medical College/Dow university of Health Sciences, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmad</FirstName>
        <LastName>Faraz</LastName>
        <affiliation locale="en_US">Karachi Medical and Dental College, Karachi, Pakistan.</affiliation>
      </Author>
      <Author>
        <FirstName>Syeda Tahira</FirstName>
        <LastName>Naqvi</LastName>
        <affiliation locale="en_US">Karachi Medical and Dental College, Karachi, Pakistan.</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete&#xA0;penetration and variable expressivity.Its most notable characteristic feature is premature synostosis of cranial sutures .The case presented is of a 4 yr old boy with box like head with microcephaly, protuberant eyes, hydrocephalus, low&#xA0;visual acquity diagnosed as a case of crouzon syndrome after clinical and radiological assessment.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/3631</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/3631/3306</pdf_url>
  </Article>
</Articles>
