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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">kpccz</journal-id><journal-title-group><journal-title xml:lang="ru">Комплексные проблемы сердечно-сосудистых заболеваний</journal-title><trans-title-group xml:lang="en"><trans-title>Complex Issues of Cardiovascular Diseases</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2306-1278</issn><issn pub-type="epub">2587-9537</issn><publisher><publisher-name>Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17802/2306-1278-2024-13-3S-208-215</article-id><article-id custom-type="elpub" pub-id-type="custom">kpccz-1485</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. Кардиология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CASE STUDY. Cardiology</subject></subj-group></article-categories><title-group><article-title>СИНДРОМ РАУХФУСА – КИСЕЛЯ У РЕБЕНКА С ДЕФЕКТОМ МЕЖПРЕДСЕРДНОЙ ПЕРЕГОРОДКИ: КЛИНИЧЕСКИЙ СЛУЧАЙ</article-title><trans-title-group xml:lang="en"><trans-title>RAUCHFUSS-KISSEL SYNDROME IN A CHILD WITH CONGENITAL HEART DEFECT. A 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/0000-0002-1352-2591</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Румянцева</surname><given-names>Александра Александровна</given-names></name><name name-style="western" xml:lang="en"><surname>Rumiantseva</surname><given-names>Alexandra A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук старший научный сотрудник лаборатории органопротекции у детей с врожденными пороками сердца федерального государственного бюджетного научного учреждения «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний», Кемерово, Российская Федерация</p></bio><bio xml:lang="en"><p>PhD, Senior Researcher at the Laboratory of Organoprotection in Children with Congenital Heart Defects, Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”, Kemerovo, Russian Federation</p></bio><email xlink:type="simple">aleksandra_1505@mail.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>Перевалова</surname><given-names>Наталья Григорьевна</given-names></name><name name-style="western" xml:lang="en"><surname>Perevalova</surname><given-names>Natalia G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>врач – детский кардиолог кардиохирургического отделения № 2 федерального государственного бюджетного научного учреждения «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний», Кемерово, Российская Федерация</p></bio><bio xml:lang="en"><p>Pediatric Cardiologist at the Cardiovascular Surgery Department №2, Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”, Kemerovo, Russian Federation</p></bio><email xlink:type="simple">pereng@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7573-0636</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коков</surname><given-names>Александр Николаевич</given-names></name><name name-style="western" xml:lang="en"><surname>Kokov</surname><given-names>Alexandr N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>доктор медицинских наук ведущий научный сотрудник лаборатории патологии кровообращения федерального государственного бюджетного научного учреждения «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний», Кемерово, Российская Федерация</p></bio><bio xml:lang="en"><p>MD, PhD, Leading Researcher at the Laboratory of Circulatory Pathology, Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”, Kemerovo, Russian Federation</p></bio><email xlink:type="simple">kokoan@kemcardio.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8076-8746</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сизова</surname><given-names>Ирина Николаевна</given-names></name><name name-style="western" xml:lang="en"><surname>Sizova</surname><given-names>Irina N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>кандидат медицинских наук научный сотрудник лаборатории пороков сердца федерального государственного бюджетного научного учреждения «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний», Кемерово, Российская Федерация</p></bio><bio xml:lang="en"><p>Researcher at the Laboratory of Heart Defects, Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”, Kemerovo, Russian Federation</p></bio><email xlink:type="simple">sizoin@kemcardio.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Федеральное государственное бюджетное научное учреждение «Научно-исследовательский институт комплексных проблем сердечно-сосудистых заболеваний»<country>Россия</country></aff><aff xml:lang="en">Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>01</day><month>11</month><year>2024</year></pub-date><volume>13</volume><issue>3S</issue><issue-title>приложение</issue-title><fpage>208</fpage><lpage>215</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Румянцева А.А., Перевалова Н.Г., Коков А.Н., Сизова И.Н., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Румянцева А.А., Перевалова Н.Г., Коков А.Н., Сизова И.Н.</copyright-holder><copyright-holder xml:lang="en">Rumiantseva A.A., Perevalova N.G., Kokov A.N., Sizova I.N.</copyright-holder><license 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.nii-kpssz.com/jour/article/view/1485">https://www.nii-kpssz.com/jour/article/view/1485</self-uri><abstract><sec><title>Основные положения</title><p>Основные положения</p><p>Описан редкий клинический случай изолированной гипоплазии верхушки левого желудочка в сочетании с врожденным пороком сердца – дефектом межпредсердной перегородки вторичного типа.</p></sec><sec><title> </title><p> </p></sec><sec><title>Резюме</title><p>Резюме</p><p>Изолированная гипоплазия верхушки левого желудочка характеризуется недоразвитием и функциональной слабостью левого желудочка. Заболевание встречается в 0,5–0,75% случаев и имеет характерные эхокардиографические и магнитно-резонансные признаки. Как правило, заболевание протекает бессимптомно, поэтому своевременные диагностика и терапия могут отсрочить возможные осложнения и улучшить качество жизни этих пациентов.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Highlights</title><p>Highlights </p><p>The review describes a rare clinical case of isolated left ventricular apical hypoplasia with atrial septal defect.</p></sec><sec><title> </title><p> </p></sec><sec><title>Abstract</title><p>Abstract</p><p>Isolated left ventricular apical hypoplasia is characterized by impaired left ventricle. The frequency of the disease is 0.5-0.75% and it can be easily detected on echocardiography. The disease is difficult to diagnose due to absence of symptoms, therefore timely diagnosis and treatment can prevent any complications and improve the quality of life.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>Синдром Раухфуса – Киселя</kwd><kwd>Изолированная гипоплазия верхушки левого желудочка</kwd><kwd>Кардиомиопатия</kwd><kwd>Хроническая сердечная недостаточность</kwd><kwd>Качество жизни</kwd><kwd>Нейрокогнитивный статус</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Rauchfuss-Kissel syndrome</kwd><kwd>Isolated left ventricular apical hypoplasia</kwd><kwd>Cardiomyopathy</kwd><kwd>Chronic heart failure</kwd><kwd>Quality of life</kwd><kwd>Neurocognitive status</kwd></kwd-group><funding-group xml:lang="ru"><funding-statement>Работа выполнена при поддержке комплексной программы фундаментальных научных исследований РАН в рамках фундаментальной темы НИИ КПССЗ № 0419-2024-0002 «Периоперационные нейропротективные стратегии в хирургии врожденных пороков сердца» при финансовой поддержке Министерства науки и высшего образования Российской Федерации в рамках национального проекта «Наука и университеты» (№ государственного учета в НИОКТР 124041800039-2).</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Подзолков В.П., Плахова В.В., Александрова С.А., Тюкина Н.С., Шляппо М.А. 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