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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">zabmedvestnik</journal-id><journal-title-group><journal-title xml:lang="ru">Забайкальский медицинский вестник</journal-title><trans-title-group xml:lang="en"><trans-title>Transbaikalian Medical Bulletin</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">1998-6173</issn><publisher><publisher-name>Читинская государственная медицинская академия</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.52485/19986173_2024_4_161</article-id><article-id custom-type="elpub" pub-id-type="custom">zabmedvestnik-364</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>НАУЧНЫЕ ОБЗОРЫ, ИЛЛЮСТРИРОВАННЫЕ КЛИНИЧЕСКИМ НАБЛЮДЕНИЕМ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SCIENTIFIC REVIEWS ILLUSTRATED WITH CLINICAL CASE STUDIES</subject></subj-group></article-categories><title-group><article-title>НЕЙТРОПЕНИИ В ПЕРИОДЕ НОВОРОЖДЕННОСТИ</article-title><trans-title-group xml:lang="en"><trans-title>NEUTROPENIA IN THE NEONATAL PERIOD: QUESTIONS REMAIN. CLINICAL CASE</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5062-1644</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Попова</surname><given-names>Н. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Popova</surname><given-names>N. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Попова  Надежда  Григорьевна,  к.м.н.,  доцент  кафедры   педиатрии</p><p>Author ID РИНЦ: 413350, Author ID Scopus: 56175513400</p><p>672000, г. Чита, ул. Горького, 39а</p></bio><bio xml:lang="en"><p>Popova N.G., Candidate of Medical Sciences, Associate Professor of Pediatric</p><p>Author ID РИНЦ: 413350, Author ID Scopus: 56175513400</p><p>39a Gorky St., Chita, Russia, 672000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7720-7339</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кочерова</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kocherova</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кочерова  Виктория Владимировна, к.м.н., доцент кафедры педиатрии</p><p>Author ID РИНЦ: 636482, Author ID Scopus: 57200200253</p><p>672000, г. Чита, ул. Горького, 39а</p></bio><bio xml:lang="en"><p>Kocherova V.V., Candidate of Medical Sciences, Associate Professor of Pediatric </p><p>Author ID РИНЦ: 636482, Author ID Scopus: 57200200253</p><p>39a Gorky St., Chita, Russia, 672000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Читинская государственная медицинская академия» Министерства здравоохранения РФ</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chita State Medical Academy</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>25</day><month>02</month><year>2025</year></pub-date><volume>0</volume><issue>4</issue><fpage>161</fpage><lpage>168</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Попова Н.Г., Кочерова В.В., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Попова Н.Г., Кочерова В.В.</copyright-holder><copyright-holder xml:lang="en">Popova N.G., Kocherova V.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.zabmedvestnik.ru/jour/article/view/364">https://www.zabmedvestnik.ru/jour/article/view/364</self-uri><abstract><p>\</p><p>Иммунодефициты в неонатальном периоде регистрируются часто. Нейтро- и лимфопении вторичного генеза выявляются при различных инфекционных заболеваниях анте-, интра- и постнатального периода инфицирования. Первичные иммунодефициты возникают вследствие генетической поломки иммунной системы и входят в синдромокомплексы наследственных и хромосомных заболеваний. Клиника иммунодефицитных состояний не имеет специфической картины и реализуется как вялотекущее инфекционное заболевание, часто приводя к сепсису. Новорожденные дети, особенно недоношенные, имеют функционально незрелую иммунную систему, при контакте с патогенами не формируют адекватный иммунный ответ, с быстрой генерализацией инфекционных заболеваний. Инфекционный процесс на фоне врожденного иммунодефицита может привести к летальному исходу. Клинический пример развития генерализованного инфекционного процесса с вторичным иммунодефицитом наглядно показывает сложность курации пациентов с летальным исходом.</p></abstract><trans-abstract xml:lang="en"><p>Immunodeficiency in the neonatal period is often recorded. Neutro- and lymphopenia of secondary genesis are detected in various infectious diseases of the ante-, intra- and postnatal period of infection. Primary immunodeficiency occurs due to genetic breakdown of the immune system and is included in the syndrome complexes of hereditary and chromosomal diseases. The clinic of immunodeficiency conditions does not have a specific picture, and is realized as a sluggish infectious disease, often leading to sepsis. Newborn children, especially premature infants, have a functionally immature immune system, do not form an adequate immune response when exposed to pathogens, which leads to rapid generalization of infectious diseases. An infectious process against the background of congenital immunodeficiency can lead to death. A clinical example of the development of a generalized infectious process with secondary immunodeficiency clearly shows the difficulty of curating patients with a fatal outcome.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>иммунодефицит</kwd><kwd>нейтропения</kwd><kwd>новорожденные дети</kwd><kwd>сепсис</kwd></kwd-group><kwd-group xml:lang="en"><kwd>immunodeficiency</kwd><kwd>neutropenia</kwd><kwd>newborn children</kwd><kwd>sepsis</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">Мухин В.Е., Панкратьева Л.Л., Милева О.И., Ярцев М.Н., Володин Н.Н. Абсолютная нейтропения и развитие инфекций в раннем неонатальном периоде у недоношенных новорожденных: одномоментное исследование. Вопросы современной педиатрии. 2020. 19. 5. 358-352. 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