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<journal>
<language>en</language>
<journal_id_issn>1726-7536</journal_id_issn>
<journal_id_issn_online>1735-8507</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi></journal_id_doi>
<journal_id_isnet></journal_id_isnet>
<journal_id_iranmedex>69</journal_id_iranmedex>
<journal_id_magiran>2139</journal_id_magiran>
<journal_id_sid>288</journal_id_sid>
<pubdate PubStatus="epublish">
	<type>gregorian</type>
	<year>2026</year>
	<month>7</month>
	<day>29</day>
</pubdate>
<volume>27</volume>
<number>1</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed></article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Inter-chromosomal Effect in a Robertsonian Translocation (13;14) Carrier with a Child Affected by Down Syndrome: A Case Report</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&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;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Down syndrome, Inter-chromosomal effect, Robertsonian translocation</keyword>
	<start_page>75</start_page>
	<end_page>80</end_page>
	<web_url>https://www.jri.ir/article/140293</web_url>
	<pdf_url>/documents/fullpaper/en/140293.pdf</pdf_url>
	<author_list><author><first_name>Sahra</first_name><middle_name></middle_name><last_name>Sahraeean</last_name><suffix></suffix><affiliation>Dr. F. Nabipour Pathobiology laboratory, Kerman, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>122972</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Asiyeh</first_name><middle_name></middle_name><last_name>Jebelli</last_name><suffix></suffix><affiliation>Department of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>122973</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Saeed</first_name><middle_name></middle_name><last_name>Ghadimi Haddadan</last_name><suffix></suffix><affiliation>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>122974</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Kobra</first_name><middle_name></middle_name><last_name>Tayyari</last_name><suffix></suffix><affiliation>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>122975</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Leila</first_name><middle_name></middle_name><last_name>Emrahi</last_name><suffix></suffix><affiliation>Legal Medicine Research Center, Iranian Legal Medicine Organization, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email>leila.emrahi@gmail.com</email><code>122976</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

