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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd"[]>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Science and Education Publishing</PublisherName>
      <JournalTitle>American Journal of Medical Sciences and Medicine</JournalTitle>
      <Issn>2327-6657</Issn>
      <Volume>2</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>11</Month>
        <Day>27</Day>
      </PubDate>
    </Journal>
    <ArticleTitle>Mosaic Double Aneuploidy with Edwards-Klinefelter Syndromes (48,XXY, +18/46XY)</ArticleTitle>
    <FirstPage>131</FirstPage>
    <LastPage>133</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Salil</FirstName>
        <LastName>Vaniawala</LastName>
      </Author>
      <Author>
        <FirstName>Pankaj</FirstName>
        <LastName>Gadhia</LastName>
        <Affiliation>Molecular Cytogenetic Unit, S.N. Gene Laboratory and Research Centre, President Plaza-A, Near RTO circle, Surat, India</Affiliation>
      </Author>
    </AuthorList>
    <ArticleIdList>
      <ArticleId IdType="pii">AJMSM2014264</ArticleId>
      <ArticleId IdType="doi">10.12691/ajmsm-2-6-4</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2014</Year>
        <Month>09</Month>
        <Day>14</Day>
      </PubDate>
      <PubDate PubStatus="revised">
        <Year>2014</Year>
        <Month>11</Month>
        <Day>21</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2014</Year>
        <Month>11</Month>
        <Day>27</Day>
      </PubDate>
    </History>
    <Abstract>Edward syndrome is rare in live births in comparison to most common Down and Patau syndromes. The estimated incidences are one in 6000 live births and interestingly 70 to 80% those affected are females. The occurrence of double aneuploidy involving XXY + 18 is very rare in live born however, most of cases are available with spontaneous abortions. Here, we report a 07 day a male infant with typical features of Edward syndrome such as microcephaly and low set of ears having mosaic double aneuploidy with Klinfelter syndrome.</Abstract>
  </Article>
</ArticleSet>