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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">10.25557/2073-7998.2020.04.66-67</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-1159</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>Митохондриальные нарушения, МРТ головного мозга и мышц конечностей при миотонической дистрофии 1 типа</article-title><trans-title-group xml:lang="en"><trans-title>Mitochondrial disorders, MRI of the brain and limb muscles in type 1 myotonic dystrophy</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>Бунак</surname><given-names>М. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Bunak</surname><given-names>M. S.</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>Котов</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotov</surname><given-names>S. V.</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>Василенко</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Vasilenko</surname><given-names>I. 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>Сидорова</surname><given-names>О. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Sidorova</surname><given-names>O. P.</given-names></name></name-alternatives><email xlink:type="simple">sidorovaop2019@mai.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>Бородатая</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Borodataya</surname><given-names>E. V.</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>Поляков</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Polyakov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГБУЗ МО «Московский областной научно-исследовательский клинический институт им. М.Ф. Владимирского»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Regional Research and Clinical Institute («MONIKI»)</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>15</day><month>09</month><year>2020</year></pub-date><volume>19</volume><issue>4</issue><fpage>66</fpage><lpage>67</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бунак М.С., Котов С.В., Василенко И.А., Сидорова О.П., Бородатая Е.В., Поляков А.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Бунак М.С., Котов С.В., Василенко И.А., Сидорова О.П., Бородатая Е.В., Поляков А.В.</copyright-holder><copyright-holder xml:lang="en">Bunak M.S., Kotov S.V., Vasilenko I.A., Sidorova O.P., Borodataya E.V., Polyakov A.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/1159">https://www.medgen-journal.ru/jour/article/view/1159</self-uri><abstract><p>При миотонической дистрофии выявлены митохондриальные нарушения, которые могут быть причиной поражения белого вещества головного мозга. При МРТ мышц конечностей у больных выявлено наиболее частое поражение - медиальная головка икроножной мышцы.</p></abstract><trans-abstract xml:lang="en"><p>In patients with myotonic dystrophy, mitochondrial disorders were detected, which could be the cause of lesions of the white matter of the brain. MRI of limb muscles in patients revealed the most frequent lesion of the medial head of the calf muscle.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>митохондрии</kwd><kwd>МРТ</kwd><kwd>миотоническая дистрофия</kwd><kwd>mitochondria</kwd><kwd>MRI</kwd><kwd>myotonic dystrophy</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>
