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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Neuromuscular Diseases</journal-id><journal-title-group><journal-title xml:lang="en">Neuromuscular Diseases</journal-title><trans-title-group xml:lang="ru"><trans-title>Нервно-мышечные болезни</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2222-8721</issn><issn publication-format="electronic">2413-0443</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">78</article-id><article-id pub-id-type="doi">10.17650/2222-8721-2012-0-2-40-51</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ORIGINAL STUDIES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Specific features of chronic inflammatory demyelinating polyneuropathy in children</article-title><trans-title-group xml:lang="ru"><trans-title>Особенности хронической воспалительной демиелинизирующей полинейропатии у детей</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kurenkov</surname><given-names>A. L.</given-names></name><name xml:lang="ru"><surname>Куренков</surname><given-names>А. Л.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>alkurenkov@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nikitin</surname><given-names>S. S.</given-names></name><name xml:lang="ru"><surname>Никитин</surname><given-names>С. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bursagova</surname><given-names>B. I.</given-names></name><name xml:lang="ru"><surname>Бурсагова</surname><given-names>Б. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kuzenkova</surname><given-names>L. M.</given-names></name><name xml:lang="ru"><surname>Кузенкова</surname><given-names>Л. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Research Center of Child Health, Russian Academy of Medical Sciences</institution></aff><aff><institution xml:lang="ru">ФБГУ Научный центр здоровья детей РАМН</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Research Institute of General Pathology and Pathophysiology, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">НИИ общей патологии и патофизиологии РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2012-04-20" publication-format="electronic"><day>20</day><month>04</month><year>2012</year></pub-date><volume>2</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>40</fpage><lpage>51</lpage><history><date date-type="received" iso-8601-date="2015-02-20"><day>20</day><month>02</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-02-20"><day>20</day><month>02</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2012, Kurenkov A.L., Nikitin S.S., Bursagova B.I., Kuzenkova L.M.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2012, Куренков А.Л., Никитин С.С., Бурсагова Б.И., Кузенкова Л.М.</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="en">Kurenkov A.L., Nikitin S.S., Bursagova B.I., Kuzenkova L.M.</copyright-holder><copyright-holder xml:lang="ru">Куренков А.Л., Никитин С.С., Бурсагова Б.И., Кузенкова Л.М.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://nmb.abvpress.ru/jour/article/view/78">https://nmb.abvpress.ru/jour/article/view/78</self-uri><abstract xml:lang="en"><p>Chronic inflammatory demyelinating polyneuropathy (CIDP) is an autoimmune peripheral neuropathy that affects both adults and children. The basis for the paper is the analysis of 5 cases of CIDP in children (3 girls and 2 boys) aged 5 to 17 years, followed up for 3 to 6 years. The types of its clinical picture and electromyographic changes at different disease stages are considered in detail. The course of the disease is traced during therapy with corticosteroids and intravenous human immunoglobulin and plasmapheresis. The results of the authors’ observations are compared with those of investigations conducted by other authors. The consideration of the diagnosis of CIDP and its treatment options focuses on that the international standards must be necessarily met to minimize errors in its differential diagnosis and management of these patients, and to make the prognosis for the disease.</p></abstract><trans-abstract xml:lang="ru"><p>Хроническая воспалительная демиелинизирующая полинейропатия (ХВДП) — заболевание периферических нервов аутоиммунной природы, поражающее как взрослых, так и детей. В основу статьи положен анализ 5 случаев ХВДП у детей в возрасте от 5 до 17 лет (3 девочки и 2 мальчика) с продолжительностью наблюдения от 3 до 6 лет. Подробно рассмотрены варианты клинической картины и электромиографических изменений на разных этапах развития заболевания. Прослежено течение заболевания на фоне терапии кортикостероидами, препаратами внутривенного иммуноглобулина человека и при использовании плазмафереза. Результаты собственных наблюдений сопоставляются с исследованиями других авторов. При рассмотрении диагностики и вариантов лечения ХВДП у детей делается акцент на необходимости обязательного соблюдения международных стандартов для минимизации ошибок в дифференциальной диагностике, ведении таких больных и формировании прогноза течения заболевания.</p></trans-abstract><kwd-group xml:lang="en"><kwd>chronic inflammatory demyelinating polyneuropathy</kwd><kwd>electromyography</kwd><kwd>intravenous human immunoglobulin therapy</kwd><kwd>corticosteroids</kwd><kwd>plasmapheresis</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>хроническая воспалительная демиелинизирующая полинейропатия</kwd><kwd>электромиография</kwd><kwd>терапия препаратами внутривенного иммуноглобулина человека</kwd><kwd>кортикостероиды</kwd><kwd>плазмаферез</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. McLeod J.G., Pollard J.D., Macaskill P. et al. 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