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<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">10.25557/2073-7998.2020.03.58-59</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-832</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>Медико-генетическое консультирование пациентов с аберрациями половых хромосом у плода</article-title><trans-title-group xml:lang="en"><trans-title>Genetic counselling for patients with fetal sex chromosome aberrations</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>Тарасова</surname><given-names>Ю. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tarasova</surname><given-names>J. A.</given-names></name></name-alternatives><email xlink:type="simple">tarasova.gen@gmail.com</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>Гнетецкая</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gnetetskaya</surname><given-names>V. A.</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>Ижевская</surname><given-names>В. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Izhevskaya</surname><given-names>V. L.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мельникова</surname><given-names>Л. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Melnikova</surname><given-names>L. L.</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>Медико-генетический центр группы компаний «Мать и дитя»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Medical Genetics center, Group of companies «Mother and child»</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><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>58</fpage><lpage>59</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Тарасова Ю.А., Гнетецкая В.А., Ижевская В.Л., Мельникова Л.Л., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Тарасова Ю.А., Гнетецкая В.А., Ижевская В.Л., Мельникова Л.Л.</copyright-holder><copyright-holder xml:lang="en">Tarasova J.A., Gnetetskaya V.A., Izhevskaya V.L., Melnikova L.L.</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/832">https://www.medgen-journal.ru/jour/article/view/832</self-uri><abstract><p>Распространение НИПТ с оценкой риска аберраций половых хромосом привело к увеличению количества пациентов, нуждающихся в генетическом консультировании в отношении этих заболеваний. Анализ факторов, влияющих на репродуктивный выбор семьи, необходим для улучшения качества предоставляемой семье информации.</p></abstract><trans-abstract xml:lang="en"><p>The spread of NIPTs with risk assessment of sex chromosome aberrations has led to an increase in the number of patients requiring genetic counselling for these pathologies. Analysis of factors influencing family reproductive choices is necessary to improve the quality of information provided to families.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>пренатальная диагностика</kwd><kwd>НИПТ</kwd><kwd>анеуплоидии половых хромосом</kwd><kwd>медико-генетическое консультирование</kwd><kwd>prenatal diagnosis</kwd><kwd>NIPT</kwd><kwd>sex chromosome aneuploidy</kwd><kwd>genetic counseling</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>
