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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">10.25557/2073-7998.2020.04.64-65</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-1158</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>Спектр наследственной патологии, характеризующейся врожденными пороками развития центральной нервной системы</article-title><trans-title-group xml:lang="en"><trans-title>Spectrum of hereditary pathology characterized by congenital brain malformations</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>Кондакова</surname><given-names>О. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Kondakova</surname><given-names>O. B.</given-names></name></name-alternatives><email xlink:type="simple">kondakovao68@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГАУ Национальный медицинский исследовательский центр здоровья детей МЗ РФ</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical Research Center for Children’s Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>15</day><month>09</month><year>2020</year></pub-date><volume>19</volume><issue>4</issue><fpage>64</fpage><lpage>65</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Кондакова О.Б., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Кондакова О.Б.</copyright-holder><copyright-holder xml:lang="en">Kondakova O.B.</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/1158">https://www.medgen-journal.ru/jour/article/view/1158</self-uri><abstract><p>Проанализирована клиническая картина у 196 пациентов с врожденными пороками развития (ВПР) головного мозга. Пациенты были обследованы с использованием методов нейровизуализации, цитогенетических и молекулярно-генетических методов. Проведен анализ спектра ВПР головного мозга. Самыми частыми ВПР головного мозга являлись аномалии церебральных комиссур, второе место занимали кортикальные мальформации, третье место - аномалии мозжечка. Хромосомная патология (включая микроделеционные синдромы) была выявлена у 19 пациентов (9,7%), моногенные болезни - у 27 пациентов (13,8%).</p></abstract><trans-abstract xml:lang="en"><p>The clinical picture in 196 patients with congenital malformations of the brain was analyzed. Patients were examined using neuroimaging techniques, cytogenetic and molecular genetics techniques. The spectrum of congenital brain defects was analyzed. The most frequent congenital malformations of the brain were abnormalities of cerebral commissures, the second place was occupied by cortical malformations, the third place - abnormalities of the cerebellum. Chromosomal pathology (including microdelection syndromes) was detected in 19 patients (9.7%), monogenic diseases in 27 patients (13.8%).</p></trans-abstract><kwd-group xml:lang="ru"><kwd>врожденный порок развития головного мозга</kwd><kwd>кортикальные мальформации</kwd><kwd>аномалии церебральных комиссур</kwd><kwd>аномалии мозжечка</kwd><kwd>congenital brain malformations</kwd><kwd>cortical malformations</kwd><kwd>cerebral commissures abnormalities</kwd><kwd>cerebellum abnormalities</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>
