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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">genort</journal-id><journal-title-group><journal-title xml:lang="ru">Гений ортопедии</journal-title><trans-title-group xml:lang="en"><trans-title>Genij Ortopedii</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1028-4427</issn><issn pub-type="epub">2542-131X</issn><publisher><publisher-name>ЦЕНТР ИЛИЗАРОВА</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18019/1028-4427-2017-23-1-80-84</article-id><article-id custom-type="elpub" pub-id-type="custom">genort-2287</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>Случай из практики</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Case report</subject></subj-group></article-categories><title-group><article-title>Синдром Марото-Лами – мукополисахаридоз VI типа: случай из практики (ошибки и осложнения)</article-title><trans-title-group xml:lang="en"><trans-title>Maroteaux-Lamy syndrome–mucopolysaccharidosis type VI: a case report (errors and complications)</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>Михайлова</surname><given-names>Л.К.</given-names></name><name name-style="western" xml:lang="en"><surname>Mikhailova</surname><given-names>L.K.</given-names></name></name-alternatives><email xlink:type="simple">cito-uchsovet@mail.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кулешов</surname><given-names>А.А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuleshov</surname><given-names>A.A.</given-names></name></name-alternatives><email xlink:type="simple">cito-spine@mail.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аржакова</surname><given-names>Н.И.</given-names></name><name name-style="western" xml:lang="en"><surname>Arzhakova</surname><given-names>N.I.</given-names></name></name-alternatives><email xlink:type="simple">cito@cito-priorov.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соколова</surname><given-names>Т.В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sokolova</surname><given-names>T.V.</given-names></name></name-alternatives><email xlink:type="simple">cito@cito-priorov.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ветрилэ</surname><given-names>М.С.</given-names></name><name name-style="western" xml:lang="en"><surname>Vetrile</surname><given-names>M.S.</given-names></name></name-alternatives><email xlink:type="simple">cito@cito-priorov.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Швачка</surname><given-names>И.В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shvachka</surname><given-names>I.V.</given-names></name></name-alternatives><email xlink:type="simple">cito@cito-priorov.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Полякова</surname><given-names>О.А.</given-names></name><name name-style="western" xml:lang="en"><surname>Poliakova</surname><given-names>O.A.</given-names></name></name-alternatives><email xlink:type="simple">beresklettt@gmail.com</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Громов</surname><given-names>И.С.</given-names></name><name name-style="western" xml:lang="en"><surname>Gromov</surname><given-names>I.S.</given-names></name></name-alternatives><email xlink:type="simple">citospine@mail.ru</email></contrib></contrib-group><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>28</day><month>03</month><year>2017</year></pub-date><volume>23</volume><issue>1</issue><issue-title>№ 1 (2017)</issue-title><fpage>80</fpage><lpage>84</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Михайлова Л., Кулешов А., Аржакова Н., Соколова Т., Ветрилэ М., Швачка И., Полякова О., Громов И., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Михайлова Л., Кулешов А., Аржакова Н., Соколова Т., Ветрилэ М., Швачка И., Полякова О., Громов И.</copyright-holder><copyright-holder xml:lang="en">Mikhailova L., Kuleshov A., Arzhakova N., Sokolova T., Vetrile M., Shvachka I., Poliakova O., Gromov I.</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.ilizarov-journal.com/jour/article/view/2287">https://www.ilizarov-journal.com/jour/article/view/2287</self-uri><abstract><p>Приводится случай мукополисахаридоза VI типа у ребенка. Низкая встречаемость мукополисахаридоза среди детского населения, трудности его дифференциальной диагностики и лечения дают основание полагать, что описание течения этого заболевания, проводившегося лечения с анализом ошибок и осложнений у ребенка 11 лет представляют интерес для ортопедов, неврологов, анестезиологов, педиатров.</p></abstract><trans-abstract xml:lang="en"><p>The authors present a case of mucopolysaccharidosis type VI in a child. Low incidence rate of mucopolysaccharidosis in pediatric population, its difficult differential diagnosis and treatment suggests that this description of the disease pathology and treatment with the analysis of errors and complications in an 11-year-old child would be of interest for orthopedists, neurologists, anesthesiologists, and pediatricians.</p></trans-abstract></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>
