﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Academy of Medical Sciences of I.R. Iran</PublisherName>
      <JournalTitle>Archives of Iranian Medicine</JournalTitle>
      <Issn>1029-2977</Issn>
      <Volume>26</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2023</Year>
        <Month>02</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Prevalence of Chromosomal Abnormalities in Iranian Patients with Infertility</ArticleTitle>
    <FirstPage>110</FirstPage>
    <LastPage>116</LastPage>
    <ELocationID EIdType="doi">10.34172/aim.2023.17</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Saima</FirstName>
        <LastName>Abbaspour</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0002-1867-4364</Identifier>
      </Author>
      <Author>
        <FirstName>Alireza</FirstName>
        <LastName>Isazadeh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8781-1177</Identifier>
      </Author>
      <Author>
        <FirstName>Matin</FirstName>
        <LastName>Heidari</LastName>
      </Author>
      <Author>
        <FirstName>Masoud</FirstName>
        <LastName>Heidari</LastName>
      </Author>
      <Author>
        <FirstName>Saba</FirstName>
        <LastName>Hajazimian</LastName>
      </Author>
      <Author>
        <FirstName>Morteza</FirstName>
        <LastName>Soleyman-Nejad</LastName>
      </Author>
      <Author>
        <FirstName>Mohammad Hossein</FirstName>
        <LastName>Taskhiri</LastName>
      </Author>
      <Author>
        <FirstName>Manzar</FirstName>
        <LastName>Bolhassani</LastName>
      </Author>
      <Author>
        <FirstName>Amir Hossein</FirstName>
        <LastName>Ebrahimi</LastName>
      </Author>
      <Author>
        <FirstName>Parvaneh</FirstName>
        <LastName>Keshavarz</LastName>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Shiri</LastName>
      </Author>
      <Author>
        <FirstName>Mansour</FirstName>
        <LastName>Heidari</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6394-0970</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/aim.2023.17</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>06</Month>
        <Day>13</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2022</Year>
        <Month>09</Month>
        <Day>13</Day>
      </PubDate>
    </History>
    <Abstract>Background: The numerical and structural abnormalities of chromosomes are the most common cause of infertility. Here, we evaluated the prevalence and types of chromosomal abnormalities in Iranian infertile patients. Methods: We enrolled 1750 couples of reproductive age with infertility, who referred to infertility clinics in Tehran during 2014- 2019, in order to perform chromosomal analysis. Peripheral blood samples were obtained from all couples and chromosomal abnormalities were evaluated by G-banded metaphase karyotyping. In some cases, the detected abnormalities were confirmed using fluorescence in-situ hybridization (FISH). Results: We detected various chromosomal abnormalities in 114/3500 (3.257%) patients with infertility. The prevalence of chromosomal abnormalities was 44/114 (38.596%) among infertile females and 70/114 (61.403%) among infertile males. Structural chromosomal abnormalities were found in 27/1750 infertile females and 35/1750 infertile males. Numerical chromosomal abnormalities were found in 17/1750 of females and 35/1750 of males. The 45, XY, rob (13;14) (p10q10) translocation and Klinefelter syndrome (47, XXY) were the most common structural and numerical chromosomal abnormalities in the Iranian infertile patients, respectively. Conclusion: In general, we found a high prevalence of chromosomal abnormalities in Iranian patients with reproductive problems. Our study highlights the importance of cytogenetic studies in infertile patients before starting infertility treatments approaches.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Chromosomal abnormalities</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Cytogenetics</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Infertility</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Karyotyping</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>