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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of PharmTech Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPTR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2249-3387</issn>
      <publisher>
        <publisher-name>undefined</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPTR31013</article-id>
      <title-group>
        <article-title>Dubowitz Syndrome- A Review</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Ramachandran</surname>
            <given-names>Sudarshan</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Vijayabala</surname>
            <given-names>G. Sree</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2013-02-01">
        <month>02</month>
        <day>01</day>
        <year>2013</year>
      </pub-date>
      <volume>3</volume>
      <issue>1</issue>
      <abstract>
        <p>Dubowitz syndrome is a genetic and chromosomal instability disorder characterized by growth hormone deficiency or defects in the cholesterol biosynthetic pathway. It is characterized by retarded growth, several craniofacial manifestations, skin eruption, soft-tissue syndactyly, central nervous system and oral manifestations. There are reports of even malignant tumors associated with this syndrome. This manuscript reviews the manifestations and management of the dubowitz syndrome.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Dubowitz</kwd>
        <kwd>Growth deficiency</kwd>
        <kwd>Malignant</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
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