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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2020.03.89-90</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-846</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КРАТКИЕ СООБЩЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BRIEF REPORT</subject></subj-group></article-categories><title-group><article-title>Частота анеуплоидии в сперматозоидах у мужчин с нарушением фертильности</article-title><trans-title-group xml:lang="en"><trans-title>The frequency of aneuploidy in sperm in men with impaired fertility</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тарлычева</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tarlycheva</surname><given-names>A. A.</given-names></name></name-alternatives><email xlink:type="simple">atarlycheva@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Маркова</surname><given-names>Ж. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Markova</surname><given-names>Zh. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сорокина</surname><given-names>Т. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Sorokina</surname><given-names>T. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Черных</surname><given-names>В. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Chernyh</surname><given-names>W. B.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шилова</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shilova</surname><given-names>N. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «Медико-генетический научный центр имени академика Н.П. Бочкова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Centre for Medical Genetics</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>01</day><month>09</month><year>2020</year></pub-date><volume>19</volume><issue>3</issue><fpage>89</fpage><lpage>90</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Тарлычева А.А., Маркова Ж.Г., Сорокина Т.М., Черных В.Б., Шилова Н.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Тарлычева А.А., Маркова Ж.Г., Сорокина Т.М., Черных В.Б., Шилова Н.В.</copyright-holder><copyright-holder xml:lang="en">Tarlycheva A.A., Markova Z.G., Sorokina T.M., Chernyh W.B., Shilova N.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.medgen-journal.ru/jour/article/view/846">https://www.medgen-journal.ru/jour/article/view/846</self-uri><abstract><p>Хромосомные аномалии (ХА), в том числе, анеуплоидии, являются одной из причин спонтанного прерывания беременности, бесплодия, рождения детей с нарушениями и пороками развития. Одним из способов оценки вероятности возникновения анеуплоидных зигот является анализ родительских гамет, однако информации об уровне анеуплоидии в таких клетках недостаточно. Был проведена оценка частоты анеуплоидии, совместимой с жизнеспособностью зигот, в ядрах сперматозоидов 82 фенотипически нормальных бесплодных мужчин с нормальным и нарушенным сперматогенезом.</p></abstract><trans-abstract xml:lang="en"><p>Chromosomal abnormalities (CA), including aneuploidy, are one of the causes of spontaneous abortion, infertility, developmental disorders and malformations. One way to evaluate probability of aneuploid zygotes occurrence is the analysis of parental gametes, however, information about the level of aneuploidy in such cells is insufficient. There was evaluated the frequency of aneuploidy compatible with the viability of the zygote in sperm nuclei of 82 phenotypically normal infertile men with normal and impaired spermatogenesis.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>нормозооспермия</kwd><kwd>олигоастенотератозооспермия</kwd><kwd>FISH сперматозоидов</kwd><kwd>анеуплоидия</kwd><kwd>normozoospermia</kwd><kwd>oligoastenoteratozoospermia</kwd><kwd>FISH</kwd><kwd>sperm aneuploidy</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
