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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">nodgo</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал детской гематологии и онкологии (РЖДГиО)</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Pediatric Hematology and Oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-1267</issn><issn pub-type="epub">2413-5496</issn><publisher><publisher-name>LTD “Graphica”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17650/2311-1267-2014-0-1-62-69</article-id><article-id custom-type="elpub" pub-id-type="custom">nodgo-15</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>Обзоры литературы</subject></subj-group></article-categories><title-group><article-title>Синдром опсоклонус-миоклонус и нейробластома (обзор литературы)</article-title><trans-title-group xml:lang="en"><trans-title>Opsoclonus-myoclonus syndrome and neuroblastoma (a review of literature)</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>Качанов</surname><given-names>Д. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kachanov</surname><given-names>D. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">totti111@list.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>Шаманская</surname><given-names>Татьяна Викторовна</given-names></name><name name-style="western" xml:lang="en"><surname>Shamanskaya</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">totti111@list.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>Малевич</surname><given-names>О. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Malevich</surname><given-names>O. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">totti111@list.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>Варфоломеева</surname><given-names>С. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Varfolomeeva</surname><given-names>S. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">totti111@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ ФНКЦ ДГОИ им. Дмитрия Рогачева Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev, Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>31</day><month>03</month><year>2015</year></pub-date><volume>0</volume><issue>1</issue><fpage>62</fpage><lpage>69</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Качанов Д.Ю., Шаманская Т.В., Малевич О.Б., Варфоломеева С.Р., 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">Качанов Д.Ю., Шаманская Т.В., Малевич О.Б., Варфоломеева С.Р.</copyright-holder><copyright-holder xml:lang="en">Kachanov D.Y., Shamanskaya T.V., Malevich O.B., Varfolomeeva S.R.</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://journal.nodgo.org/jour/article/view/15">https://journal.nodgo.org/jour/article/view/15</self-uri><abstract><p>Синдром опсоклонус-миоклонус (ОМС) является редким неврологическим синдромом. Длительное существование неврологических симптомов у пациентов без должного проведенного обследования и лечения, ошибки в диагнозе при первичном обращении больных свидетельствуют о том, что большинство врачей не осведомлены о данном синдроме и критериях его диагностики. Педиатр, который наблюдает ребенка раннего возраста с мозжечковой атаксией, должен знать о том, что это состояние может быть проявлением ОМС. С нейробластомой (НБ) ассоциированы 50 % случаев ОМС, развившегося в детском возрасте. Однако до настоящего времени возникают трудности в ранней диагностике этого состояния, определении объема инициального обследования и тактики терапии. В данной статье приведен обзор литературы, посвященный различным аспектам патогенеза, диагностики, клиники, лечения и прогноза при ОМС. Отдельно рассмотрены вопросы, посвященные ОМС, ассоциированному с НБ.</p></abstract><trans-abstract xml:lang="en"><p>Opsoclonus-myoclonus syndrome (OMS) is a rare neurological disorder. Chronic neurological symptoms in patients, improperly examined and treated, and diagnostic errors during their first visit to a doctor suggest that most physicians are unaware of this syndrome and criteria for its diagnosis. The pediatrician who follows up an infant with cerebellar ataxia must know that this condition may be a manifestation of OMS. 50 % of childhood-onset OMS cases are associated with neuroblastoma (NB). However, to date difficulties have emerged in the early diagnosis of this condition and in the determination of initial examination scope and therapy policy. This paper reviews the literature on different aspects of the pathogenesis, diagnosis, clinical presentation, treatment, and prognosis of OMS. The issues of NB-associated OMS are considered separately.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>синдром опсоклонус-миоклонус</kwd><kwd>нейробластома</kwd><kwd>дети</kwd></kwd-group><kwd-group xml:lang="en"><kwd>opsoclonus myoclonus syndrome</kwd><kwd>neuroblastoma</kwd><kwd>children</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Kinsbourn М. Myoclonic encephalopathy of Infants. J Neurol Neurosurg Psychiatr 1962;25:271.</mixed-citation><mixed-citation xml:lang="en">Kinsbourn М. Myoclonic encephalopathy of Infants. J Neurol Neurosurg Psychiatr 1962;25:271.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Rothenberg A. B., Berdon W. E., D’Angio G. J. et al. The association between neuroblastoma and opsoclonus-myoclonus syndrome: a historical review. 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