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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">J Reprod Infert</journal-id>
      <journal-id journal-id-type="publisher-id">arij001</journal-id>
      <journal-title-group>
        <journal-title>Journal of Reproduction &amp; Infertility</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2228-5482</issn>
      <issn pub-type="epub">2251-676X</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">jri140293</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Inter-chromosomal Effect in a Robertsonian Translocation (13;14) Carrier with a Child Affected by Down Syndrome: A Case Report</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Sahraeean</surname><given-names>Sahra</given-names></name></contrib><aff>Dr. F. Nabipour Pathobiology laboratory, Kerman, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Jebelli</surname><given-names>Asiyeh</given-names></name></contrib><aff>Department of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ghadimi Haddadan</surname><given-names>Saeed</given-names></name></contrib><aff>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Tayyari</surname><given-names>Kobra</given-names></name></contrib><aff>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Emrahi</surname><given-names>Leila</given-names></name></contrib><aff>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</aff></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>27</volume>
      <issue>1</issue>
      <fpage>75</fpage>
      <lpage>80</lpage>
      <history>
        <date date-type="received">
          <day>10</day>
          <month>1</month>
          <year>2026</year>
        </date>
        <date date-type="accepted">
          <day>16</day>
          <month>5</month>
          <year>2026</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p&gt;Background: Although the balanced carriers of Robertsonian translocations (ROBs) typically exhibit normal phenotypes, they may experience recurrent abortions or have offspring with chromosomal disorders. A proposed mechanism is the inter-chromosomal effect (ICE), where disrupted meiotic segregation may increase aneuploid gamete production. This study presents a male case carrier of t(13;14) who had a deceased child with Down syndrome (DS) and investigates t(13;14) as a potential factor contributing to the birth of a child with DS.&lt;br /&gt;
Case Presentation: A couple with a history of recurrent abortions and a deceased child with DS was referred to a medical genetics laboratory. Karyotype analysis revealed that the male partner was a carrier of t(13;14) (45,XY,t(13;14)), while the female partner had a normal karyotype. The couple&amp;rsquo;s subsequent pregnancy resulted in a healthy female fetus inheriting t(13;14). The deceased child had a karyotype of 47, XY, +21, consistent with DS. In this study, the role of t(13;14) and ICE as potential contributors to the birth of a child with DS was explored.&lt;br /&gt;
Conclusion: Prenatal screening for carriers of ROBs is strongly recommended to assess the risk of unbalanced chromosomal disorders in offspring.&lt;/p&gt;

      </p>
      </abstract>
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