<?xml version="1.0" encoding="UTF-8"?>
<!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">10.25557/2073-7998.2020.03.51-52</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-829</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>Хромосомные аномалии при кистозных образованиях брюшной полости у плода в первом триместре беременности</article-title><trans-title-group xml:lang="en"><trans-title>Chromosomal abnormalities in the first-trimester fetuses with abdominal cysts</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>Новикова</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Novikova</surname><given-names>I. V.</given-names></name></name-alternatives><email xlink:type="simple">i.novikova@mail.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>Венчикова</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Venchikova</surname><given-names>N. A.</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>Республиканский научно-практический центр «Мать и дитя» Министерства здравоохранения Республики Беларусь</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Republican Scientific-Practical Centre “Mother and Child”</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>51</fpage><lpage>52</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Новикова И.В., Венчикова Н.А., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Новикова И.В., Венчикова Н.А.</copyright-holder><copyright-holder xml:lang="en">Novikova I.V., Venchikova N.A.</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/829">https://www.medgen-journal.ru/jour/article/view/829</self-uri><abstract><p>Проведено изучение частоты и спектра хромосомных аномалий (ХА) у 76 плодов при кистозных образованиях брюшной полости и малого таза, выявленных при пренатальном скрининге в I триместре беременности. Спектр патологических образований составили киста холедоха, атрезии двенадцатиперстной и прямой кишки/ануса, дисгенезия клоаки и мегацистис. Наряду с атрезиями желудочно-кишечного тракта и мочевых путей, в I триместре выявляются и другие патологические состояния: гетеротаксия и правосторонняя диафрагмальная грыжа. Частота ХА при выявлении у плода кистозных образований брюшной полости и малого таза в ранние сроки беременности в среднем составляет 23,7%.</p></abstract><trans-abstract xml:lang="en"><p>First-trimester aborted fetuses with abdominal cysts (n=76) have been examined at anatomic-pathological investigation. A final diagnosis included choledochal cyst, duodenal and anorectal atresia, cloacal disgenesis syndrome and megacystis. Besides gastrointestinal atresia and lower urinary tract obstructions heterotaxy and diaphragmatic hernia have been revealed at morphological examination. In total 23,7% of fetal abdominal cysts in the first trimester of gestation were associated with chromosomal abnormalities.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хромосомные аномалии</kwd><kwd>кисты брюшной полости</kwd><kwd>плод</kwd><kwd>мегацистис</kwd><kwd>I триместр беременности</kwd><kwd>chromosomal abnormality</kwd><kwd>abdominal cysts</kwd><kwd>fetus</kwd><kwd>megacystis</kwd><kwd>first trimester</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>
