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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">nid</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология и диализ</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology and Dialysis</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1680-4422</issn><issn pub-type="epub">2618-9801</issn><publisher><publisher-name>Российское диализное общество</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">nid-1551</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 И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Полиморфизм генов ренин-ангиотензин-альдостероновой системы при нефротическом синдроме у детей (Обзор литературы)</article-title><trans-title-group xml:lang="en"><trans-title>Renin-angiotensin-aldosterone system gene polymorphism in children with nephrotic syndrome Review</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>Шарнова</surname><given-names>Ж. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Sharnova</surname><given-names>Zh. P.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Цыгин</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsygin</surname><given-names>A. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Тихомиров</surname><given-names>Е. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Tikhomirov</surname><given-names>E. E.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>НИИ педиатрии НЦЗД РАМН, г. Москва</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2006</year></pub-date><pub-date pub-type="epub"><day>23</day><month>06</month><year>2025</year></pub-date><volume>8</volume><issue>3</issue><fpage>216</fpage><lpage>224</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шарнова Ж.П., Цыгин А.Н., Тихомиров Е.Е., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Шарнова Ж.П., Цыгин А.Н., Тихомиров Е.Е.</copyright-holder><copyright-holder xml:lang="en">Sharnova Z.P., Tsygin A.N., Tikhomirov E.E.</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.nephro.ru/jour/article/view/1551">https://journal.nephro.ru/jour/article/view/1551</self-uri><abstract><p>Нефротический синдром (НС), объединяющий гетерогенную группу гломерулярных заболеваний, является одной из актуальных проблем детской нефрологии. Заболеваемость первичным НС составляет 2-13 случаев на 100 000 детей в возрасте до 10 лет [<xref ref-type="bibr" rid="cit1">1</xref>]. Постоянное увеличение числа нефротических больных, прогрессирующих до стадии терминальной почечной недостаточности (ТПН) и нуждающихся в заместительной почечной терапии - лечении хроническим или перитонеальным диализом - или в трансплантации почки [<xref ref-type="bibr" rid="cit2">2</xref>], убеждает в необходимости включения проблемы НС в список приоритетных исследований в нефрологии.</p></abstract><kwd-group xml:lang="ru"><kwd>обзор</kwd><kwd>нефротический синдром</kwd><kwd>хроническая почечная недостаточность</kwd><kwd>полиморфизм генов</kwd><kwd>ренин-ангиотензин-альдостероновая система</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">Баранов А.А. Клинические рекомендации по педиатрии. 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